Craniosynostosis

Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification),<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> thereby changing the growth pattern of the skull.<ref name="Brief Review">Template:Cite journal</ref> Because the skull cannot expand perpendicular to the fused suture, it compensates by growing more in the direction parallel to the closed sutures.<ref name="Brief Review" /> Sometimes the resulting growth pattern provides the necessary space for the growing brain, but results in an abnormal head shape and abnormal facial features.<ref name="Brief Review" /> In cases in which the compensation does not effectively provide enough space for the growing brain, craniosynostosis results in increased intracranial pressure leading possibly to visual impairment, sleeping impairment, eating difficulties, or an impairment of mental development combined with a significant reduction in IQ.<ref name="Intracranial pressure">Template:Cite journal</ref>

Craniosynostosis occurs in one in 2000 births. Craniosynostosis is part of a syndrome in 15% to 40% of affected patients, but it usually occurs as an isolated condition.<ref name="Bannink">Template:Cite journal</ref><ref name="genetics">Template:Cite journal</ref> The term is from cranio, cranium; + syn, together; + ost, relating to bone; + osis, denoting a condition. Craniosynostosis is the opposite of metopism.

Signs and symptoms

File:Single suture synostosis.png

Kinds of craniosynostosis

Children born with craniosynostosis have a distinct phenotype, i.e., appearance—observable traits caused by the expression of a condition's genes. The features of craniosynostosis' particular phenotype are determined by which suture is closed.<ref name="Kabbani H">Template:Cite journal</ref> The fusion of this suture causes a certain change in the shape of the skull; a deformity of the skull.<ref name="Kabbani H"/>

Virchow's law dictates that, when premature suture closure occurs, growth of the skull typically is restricted perpendicularly to the fused suture and enhanced in a plane parallel to it, thus trying to provide space for the fast-growing brain.<ref name="Cranial vault growth">Template:Cite journal</ref> Using this law, the pattern of skull deformity in craniosynostosis often may be predicted.<ref name="Cranial vault growth"/>

Scaphocephaly

An illustrative example of this phenomenon is scaphocephaly, which translates from Greek as 'boat-head'; the name of the condition is suggestive of the shape of the affected skull. A synonymous term is 'dolichocephaly' (the prefix 'dolicho-' means elongated).<ref>Template:Cite journal</ref>

Premature sagittal suture closure restricts growth in a perpendicular plane, thus the head will not grow sideways and will remain narrow.<ref name="Neurodevelopment"/><ref name="Persing et al">Template:Cite journal</ref> This is best seen in a view standing above the child looking downward at the top of the head.<ref name="cunningham"/> Compensatory growth occurs forward at the coronal suture and backward at the lambdoid suture giving respectively a prominent forehead, called frontal bossing, and a prominent back portion of the head, called coning.<ref name="Neurodevelopment"/><ref name="Persing et al"/> This is the most common form of craniosynostosis.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Trigonocephaly

Trigonocephaly is a result from the premature closure of the metopic suture.<ref name="Neurodevelopment"/><ref name="Persing et al"/> According to Virchow's law, this fusion will result in a narrow forehead, which is even further emphasized by ridging of the suture.<ref name="Neurodevelopment"/><ref name="Persing et al"/> Compensatory growth occurs at both the coronal sutures, thereby pushing the forehead forwards.<ref name="Neurodevelopment"/><ref name="Persing et al"/> The resulting shape appears triangular from above.<ref name="cunningham"/> Like many medical terms, 'trigonocephaly' is derived from Greek, and indicates the head in question is triangular in shape. A facial feature of metopic synostosis is hypotelorism; in the frontal view, it can be seen that the width between the eyes is smaller than usual.<ref name="Persing et al"/>

Plagiocephaly

File:Плагиоцефалия.jpg

Head of plagiocephalic baby viewed from above

The Greek word πλάγιος plágios means "skew". Plagiocephaly can be subclassified as anterior plagiocephaly or posterior plagiocephaly.Template:Citation needed

Anterior plagiocephaly

Anterior plagiocephaly is a clinical description of unilateral coronal synostosis.<ref name="Neurodevelopment"/><ref name="Persing et al"/> Children born with unilateral coronal synostosis develop due to compensatory mechanisms a skew head; a plagiocephaly.<ref name="Neurodevelopment"/><ref name="Persing et al"/>

The sagittal suture 'divides' the coronal suture in two halves; unilateral meaning that either the right side or the left side to the sagittal suture is fused. This fact immediately raises an important point. Unlike closure of the sagittal or the metopic suture, right and left are not the same in unilateral coronal synostosis.<ref name="Neurodevelopment"/><ref name="Persing et al"/> This asymmetry shows in the skull deformity, as well as in the facial deformity and the complications.<ref name="Neurodevelopment"/><ref name="Persing et al"/>

This time, the skull deformity can only partly be predicted using Virchow's law. Growth is arrested in the plane perpendicular to the fused suture and the forehead is flattened, but only at the ipsilateral side of the head.<ref name="Neurodevelopment"/><ref name="Persing et al"/> Ipsilateral indicates the same side of the head as where the suture is closed. Compensatory growth occurs in a parallel plane, as well as in a perpendicular plane.<ref name="Neurodevelopment"/><ref name="Persing et al"/> An increase in growth at the metopic and the sagittal suture accounts for the parallel plane and will result in bulging at the temporal fossa.<ref name="Neurodevelopment"/><ref name="Persing et al"/> Compensatory growth in the perpendicular plane occurs on the side of the head with the patent coronal suture, the contralateral side.<ref name="Neurodevelopment"/><ref name="Persing et al"/> Half of the forehead will bulge forwards.

Assessment of the skull from a top view shows asymmetry of the frontal bones, an increased width of the skull and a forward displacement of the ear at the ipsilateral side of the head.<ref name="cunningham"/> Assessment of the skull from a frontal view will show asymmetrical features of the face, including a displacement of the chin point of the jaw and a deviation of the tip of the nose.<ref name="Neurodevelopment"/><ref name="Persing et al"/> The chin point is located more to the contralateral side of the head, due to the ipsilateral forward displacement of the temporomandibular joint together with the ear.<ref name="Neurodevelopment"/><ref name="Persing et al"/> The tip of the nose will also point towards the contralateral side.<ref name="Neurodevelopment"/><ref name="Persing et al"/> Complications based on the skull deformation include malocclusion of the jaw, in as many as 90%; a subtle form of strabismus, caused by the asymmetrical placement of the orbits;<ref name="Persing et al"/> and refractive error, particularly astigmatism, due to asymmetrical development of the orbits.<ref>Template:Cite journal</ref>

Posterior plagiocephaly

Unilateral lambdoid synostosis is also called posterior plagiocephaly, indicating that this gives, just like unilateral coronal synostosis, a 'skew head'. The difference is that this time, the deformity mostly shows at the occiput.Template:Citation needed

By Virchow's law, restriction of growth will occur at the ipsilateral side of the head; compensatory growth will occur at the contralateral side of the head. This growth pattern exerts an effect at the base of the skull, which is not even when the child is assessed from a point of view standing behind the child, as well as on the cervical spine, which shows a curvature.<ref name="Huang">Template:Cite journal</ref> In addition, from a point of view standing behind the child, a bulging of the mastoid can be seen.<ref name="Huang"/> Minimal forehead asymmetries are typically seen.<ref name="Persing et al"/>

Brachycephaly

Brachycephaly, or a 'short head', is the result of a closure of both the coronal sutures.<ref name="Persing et al"/> Following Virchow's law, this will result in a child's head with a restriction of growth in the forward direction and in the backward direction: recessed frontal bones and a flattened occiput.<ref name="Persing et al"/> Compensatory growth will occur sideways, due to the sagittal suture, and upwards, due to the lambdoid sutures.<ref name="Persing et al"/>

Turricephaly

Turricephaly, also known as oxycephaly, acrocephaly, and high-head syndrome, is a type of cephalic disorder. This is a term sometimes used to describe the premature closure of the coronal suture plus any other suture, like the lambdoid suture.Template:Citation needed

Pansynostosis

The word pansynostosis is also Greek-derived and can be translated as "all one bone", indicating that all of the sutures are closed.<ref name="Chumas PD">Template:Cite journal</ref> In general practice, the term is used to describe the children with three or more cranial sutures closed.<ref name="Chumas PD"/>

Pansynostosis can present in several ways. The appearance can be the same as that seen with primary microcephaly: a markedly small head, but with normal proportions.<ref name="Pansynostosis"/> The most severe form of pansynostosis is kleeblattschädel (cloverleaf skull), which presents with bulging of the different bones of the cranial vault.<ref name="Pansynostosis"/><ref>Template:Cite journal</ref>

Kleeblattschädel is a feature of several conditions and can also be seen in nonsyndromic manifestations. True pansynostosis can also be nonsyndromic<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> but is also seen in two conditions: ERF-related craniosynostosis and Robinow-Sorauf syndrome (now considered a form of Saethre-Chotzen syndrome).<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Other forms

• Apert syndrome: an abnormal skull shape, small upper jaw, and fusion of the fingers and toes.
• Baller-Gerold syndrome: craniosynostosis with radial aplasia.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web }}</ref>

• Beare-Stevenson syndrome: craniosynostosis with cutis gyrata, acanthosis nigricans, and digit anomalies.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web }}</ref>

• Carpenter syndrome: acrocephaly with variable synostosis of the sagittal, lambdoid, and coronal sutures; peculiar facies, brachydactyly and syndactyly, foot polydactyly.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web }}</ref>

• Crouzon syndrome: craniofacial abnormalities with bilateral coronal suture fusion; anterior and posterior of skull shortness, flat cheek bones and a flat nose.
• Jackson-Weiss syndrome: craniosynostosis with midfacial hypoplasia and foot anomalies.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web }}</ref>

• Muenke syndrome: coronal craniosynostosis (plagiocephaly and brachycephaly), short feet and palms, hearing impairment, hypertelorism, and proptosis.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web }}</ref>

• Pfeiffer syndrome: abnormalities of the skull, hands, and feet; wide-set, bulging eyes, an underdeveloped upper jaw, beaked nose.
• Saethre–Chotzen syndrome: short or broad head; the eyes may be spaced wide apart and have palpebral ptosis (droopy eyelids), and fingers maybe abnormally short and webbed.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web }}</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

• Shprintzen-Goldberg syndrome: craniosynostosis with marfanoid habitus and tissue anomalies.<ref>{{#invoke:citation/CS1|citation

|CitationClass=web

}}</ref>

• Précis de psychiatrie 3.jpg

  Apert syndrome

• Carpenter Syndrome 1.jpg

  Carpenter syndrome

• Patient with Crouzon syndrome (1912).jpg

  Crouzon syndrome

• Osseous Deformity Case 1.jpg

  Muenke syndrome

• Girl aged 17 years with marked proptosis Wellcome L0062481.jpg

  Pfeiffer syndrome

• Pyrgocephalus.jpg

  Saethre-Chotzen syndrome

Complications

Not all cranial abnormalities seen in children with craniosynostosis are solely a consequence of the premature fusion of a cranial suture. This is especially true in the cases with syndromic craniosynostosis. Findings include elevation of the intracranial pressure; obstructive sleep apnea (OSA); abnormalities in the skull base and neurobehavioral impairment.<ref name="Persing et al"/>

Elevated intracranial pressure

When the ICP is elevated the following symptomes may occur: vomiting, visual disturbance, bulging of the anterior fontanel, altered mental status, papilledema and headache.<ref name="jong">Template:Cite journal</ref>

The main risks of prolonged elevated intracranial pressure may include cognitive impairment and impaired vision through prolonged papilledema<ref name="Pansynostosis"/> and subsequent optic atrophy.<ref>Template:Cite journal</ref> These are the main reasons why fundoscopy should be performed during the physical examination of children with craniosynostosis.<ref name="Pansynostosis"/>

The causes of an elevation of the intracranial pressure are best understood using the Monro-Kellie doctrine.<ref name="Mokri">Template:Cite journal</ref> The Monro-Kellie doctrine reduces the cranial vault to a box with rigid walls.<ref name="Mokri"/> This box contains three elements: brain, intracranial blood and cerebrospinal fluid.<ref name="Mokri"/> The sum of volumes of these three elements is constant.<ref name="Mokri"/> An increase in one should cause a decrease in one or both of the remaining two, thereby preventing an elevation of the intracranial pressure.<ref name="Mokri"/>

A compensatory mechanism involves the movement of cerebrospinal fluid from the cranial vault towards the spinal cord.<ref name="Mokri"/> The volume of blood in the cranial vault is auto-regulated by the brain, and will therefore not decrease that easily.<ref name="Mokri"/>

Intracranial pressure will rise as a result of continued brain growth within the rigid skull.<ref name="Pansynostosis"/> It appears that in children with craniosynostosis, the expected decrease of intracranial blood is probably not occurring as it should according to the Monro-Kellie hypothesis.<ref name="Tamburrini"/> This is shown when the brain expands in the fixed skull, which gives a faster rise in intracranial pressure than would be expected.<ref name="Tamburrini"/>

Obstructive sleep apnea

The short stops in breathing during the sleep are the mainstay of OSA. Other symptoms can be difficulty in breathing, snoring, day-time sleepiness and perspiration.<ref name="Bannink"/> The main causative agent of OSA is the [midface hypoplasia], which also poses a risk to the eyes that can be seen bulging out of the eye sockets. Other factors, such as a micrognathism and adenoid hypertrophy, are likely to contribute in causing OSA.<ref name="Bannink"/> The most common syndromic forms of craniosynostosis; i.e. Apert, Crouzon and Pfeiffer, have an increased risk of developing OSA. The children have nearly 50% chance of developing this condition.<ref name="Bannink"/>

A theory regarding the involvement of OSA as a causative agent for elevated intracranial pressure suggests an association with the auto-regulation of blood flow in the brain.<ref name="Bristol"/> Certain cells in the brain respond specifically to an increase of Template:CO2 in the blood.<ref name="Intracranial pressure"/><ref name="Eide">Template:Cite journal</ref> The response involves vasodilatation of the cranial vault blood vessels, increasing the volume of one of the elements in the Monro-Kellie doctrine.<ref name="Intracranial pressure"/><ref name="Eide"/> The increase of Template:CO2 concentration in the blood is a consequence of impaired breathing, especially seen when the child with OSA is sleeping.<ref name="Intracranial pressure"/><ref name="Eide"/> It is well documented that the highest spikes in intracranial pressure often occur during sleep.<ref name="Intracranial pressure"/><ref name="Eide"/>

Abnormalities in the skull base

Impaired venous outflow is often caused by a hypoplastic jugular foramen.<ref name="Bristol"/> This causes an increase in the intracranial blood volume, thereby causing an increase in intracranial pressure.<ref name="Bristol"/>

This can be further complicated with a possible Arnold–Chiari malformation, which can partially obstruct the flow of cerebro-spinal fluid from the neurocranium to the spinal cord.<ref name="genetics"/> The Chiari malformation may be asymptomatic or present with ataxia, spasticity or abnormalities in breathing, swallowing or sleeping.<ref name="genetics"/>

Due to the impaired venous outflow, which may be further complicated with an Arnold–Chiari malformation, there is often a clinical image of hydrocephalus present. Hydrocephalus is seen in 6.5 to 8% of patients with Apert's syndrome, 25.6% in patients with Crouzon's syndrome and 27.8% of those with Pfeifer's syndrome.<ref name="Cohen">Template:Cite book</ref> Ventriculomegaly is a usual finding in children with the Apert syndrome.<ref name="Collmann">Template:Cite journal</ref>

Neurobehavioural impairment

Neurobehavioural impairment includes problems with attention and planning, processing speed, visual spatial skills, language, reading and spelling.<ref name="Neurodevelopment"/> A decreased IQ may also be part of the problems.<ref name="Neurodevelopment"/>

It has been suggested that these problems are caused by a primary malformation of the brain, rather than being a consequence of the growth restriction of the skull and elevated intracranial pressure. Some evidence for this statement has been provided by studies using computed tomographic (CT) scans and magnetic resonance imaging (MRI) to identify differences between the structures of the brains of healthy children and those affected with craniosynostosis.<ref name="Neurodevelopment"/> It has been found that corrective surgery of the cranial vault alters the morphology of the brain compared with the situation before surgical intervention.<ref name="Neurodevelopment"/> However the structure was still abnormal in comparison to children without craniosynostosis.<ref name="Neurodevelopment"/>

Causes

Advances in the fields of molecular biology and genetics, as well as the use of animal models have been of great importance in expanding our knowledge of suture fusion.<ref name="Brief Review"/> Research in animal models has led to the idea that the dura mater plays an important role in determining closure or patency of the suture.<ref name="Brief Review"/> In contrast to the dura mater it appears that the periosteum is not essential in causing closure or patency.<ref name="Brief Review"/>

File:Suturefusion2.jpg

Gene expression pattern during cranial suture fusion

Instead of describing the abnormalities in structure and form, research focuses nowadays at decoding the molecular interactions that underlie them.<ref name="Brief Review"/> Detailed work by Sahar et al at Stanford University using chip microarray and quantitative real-time PCR on samples of suture junctions during development, reveals cranial suture fusion in mammals is a tightly orchestrated expression of genes in specific temporal order, leading to endochondral ossification.<ref>Sahar DE, Longaker MT, Quarto N. Sox9 neural crest determinant gene controls patterning and closure of the posterior frontal cranial suture. Dev Biol. 2005 Apr 15;280(2):344-61.</ref> Sox9, Slug, Osteocalcin, growth factors and multiple Collagen type genes are upregulated in this coordinated and specific sequence (see Figure). Despite the progress that has been made, many things are still not understood about the suture biology and the exact causative pathways remain yet to be completely understood.<ref>Template:Cite journal</ref>

Multiple potential causes of premature suture closure have been identified, such as the several genetic mutations that are associated with syndromic craniosynostosis.<ref name="Brief Review"/> The cause of nonsyndromic craniosynostosis however, is still greatly unknown.<ref name="Neurodevelopment">Template:Cite journal</ref> Most likely, a role is played by biomechanical factors, as well as environmental, hormonal and genetical factors.<ref name="Neurodevelopment"/>

New insights have given fuel to a debate whether there might be an intrinsic factor causing the premature fusion of the sutures. Brain structures of children with craniosynostosis were evaluated using magnetic resonance imaging.<ref name="Neurodevelopment"/> Differences were seen compared with the brain structures of normal children.<ref name="Neurodevelopment"/> The question now is whether these differences are caused by the craniosynostosis, or are the cause of craniosynostosis.Template:Citation needed

Biomechanical factors

Biomechanical factors include fetal head constraint during pregnancy.<ref name="Expression of Indian Hedgehog">Template:Cite journal</ref> It has been found by Jacob et al. that constraint inside the womb is associated with decreased expression of Indian hedgehog protein and noggin. These last two are both important factors influencing bone development.<ref name="Expression of Indian Hedgehog"/>

Environmental factors

Environmental factors refer for example to maternal smoking and the maternal exposure to amine-containing drugs. Several research groups have found evidence that these environmental factors are responsible for an increase in the risk of craniosynostosis, likely through effects on fibroblast growth factor receptor genes.<ref name="Carmicheal SL et al.c">Template:Cite journal</ref><ref name="Gardner">Template:Cite journal</ref><ref name="Honein MA et al.">Template:Cite journal</ref><ref name="Källén K et al.">Template:Cite journal</ref><ref name="Olshan">Template:Cite journal</ref>

On the other hand, a recent evaluation of valproic acid (an anti-epilepticum), which has been implicated as a causative agent, has shown no association with craniosynostosis.<ref name="Valproic">Template:Cite journal</ref>

Certain medication (like amine-containing drugs) can increase the risk of craniosynostosis when taken during pregnancy, these are so-called teratogenic factors.<ref name="Gardner"/><ref name="Olshan"/>

Hormonal factors

Hyperthyroid induced craniosynostosis is a hormone mediated premature closure.<ref name="Premature craniosynostosisc">Template:Cite journal</ref> It is thought that the bone matures faster due to high levels of thyroid hormone.<ref name="Premature craniosynostosisc"/>

Genetic factors

In 6 to 11% of the children born with coronal synostosis, more often involving the bilateral cases than unilateral, other members of the family have been reported that were also born with the same condition.<ref name="Molecular analysisc">Template:Cite journal</ref> This finding is highly suggestive of a genetic cause, which has possibly been found in the fibroblast growth factor receptor 3 (FGFR3) and TWIST genes.<ref name="Molecular analysisc"/>

Fibroblast growth factor and fibroblast growth factor receptors regulate fetal bone growth and are expressed in cranial sutures during pregnancy.<ref name="genetics"/> The transcription factor gene TWIST is thought to decrease the function of FGFR, thus also indirectly regulating fetal bone growth.<ref name="genetics"/> A relation between the mutations in these genes and craniosynostosis is therefore possible. Moloney et al. observed a FGFR3 mutation in as many as 31% of the cases with nonsyndromic coronal synostosis, thus showing that FGFR abnormalities play an important role in nonsyndromic craniosynostosis.<ref name="Prevalence of">Template:Cite journal</ref>

In terms of syndromic craniosynostosis not only do FGFR3 and TWIST genes feature, but also FGFR1 and in particular FGFR2, which has been reported in 90% of the syndromic craniosynostoses such as Apert, Crouzon, Peiffer and Jackson–Weiss.<ref name="pmid18391498">Template:Cite journal</ref><ref name="Cranial suture biology">Template:Cite journal</ref><ref name="Craniosynostosis: genes and mechanisms">Template:Cite journal</ref> The mutations can be divided into mutations that lead to gain of function (in FGFR genes) and mutations that lead to loss of function (in TWIST genes).<ref name="Cranial suture biology"/><ref name="Craniosynostosis: genes and mechanisms"/> Craniosynostosis is therefore likely the result of a disturbance in the fine balance that regulates the multiplication and maturation of the precursor bone cells in the cranial sutures.<ref name="Brief Review"/>

The familial rate, which is different for nonsyndromic and syndromic cases, provides an important clue.<ref name="Hunter">Template:Cite journal</ref><ref name="Lajeunie">Template:Cite journal</ref> In the nonsyndromic cases, a positive family history is found in 2% of the cases with sagittal suture closure<ref name="Hunter"/><ref name="Lajeunie"/> and in 6% to 11% of the cases with coronal suture closure.

Cranial sutures

The mesenchyme above the meninges undergoes intramembranous ossification forming the neurocranium.<ref name="Brief Review"/> The neurocranium consists of several bones, which are united and at the same time separated by fibrous sutures.<ref name="Brief Review"/> This allows movement of the separate bones in relation to one another; the infant skull is still malleable.<ref name="Brief Review"/> The fibrous sutures specifically allow the deformation of the skull during birth<ref name="Brief Review"/> and absorb mechanical forces during childhood<ref name="genetics"/> They also allow the necessary expansion during brain growth.<ref name="Brief Review"/>

In the very first years of life the sutures serve as the most important centers of growth in the skull.<ref name="Brief Review"/> The growth of the brain and the patency of the sutures depend on each other.<ref name="Management of craniosynostosis">Template:Cite journal</ref> Brain growth pushes the two sides of the patent sutures away from each other, thereby enabling growth of the neurocranium.<ref name="Management of craniosynostosis"/> This means that the neurocranium can only grow if the sutures remain open.<ref name="Management of craniosynostosis"/> The neurocranium will not grow when the forces induced by brain growth are not there.<ref name="cunningham">Template:Cite journal</ref> This will occur for example when the intracranial pressure drops; the sutures do not experience stretching anymore causing them to fuse.<ref name="Pansynostosis">Template:Cite journal</ref>

Diagnosis

The evaluation of a child suspected to have craniosynostosis is preferentially performed in a craniofacial center. The three main elements of analysis include medical history, physical examination and radiographic analysis.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Medical history should in any case include questions about risk factors during pregnancy, the familial rate and the presence of symptoms of elevated intracranial pressure (ICP).Template:Citation needed

Elevated ICP

• Symptoms of increased intracranial pressure – such as headache and vomiting – should be questioned after.<ref name="Tamburrini">Template:Cite journal</ref><ref name="Bristol">Template:Cite journal</ref> An elevation of ICP can be present in 4 to 20% of the children where only a single suture is affected.<ref name="Tamburrini"/><ref name="Bristol"/> The incidence of ICP in children with more than one suture involved can be as high as 62%.<ref name="Renier">Template:Cite journal</ref> However, even though the children are affected, symptoms are not always present.Template:Citation needed

Physical examination

Fundoscopy should always be performed in children with craniosynostosis.<ref name="Papilledema">Template:Cite journal</ref> It is used to find papilledema which is sometimes the only symptom of elevated intracranial pressure shown in these children.<ref name="Papilledema"/>

Other parts of the physical examination include the measurement of the head circumference, the assessment of the skull deformity and the search for deformities affecting other parts of the body.<ref name="Pansynostosis"/> The head circumference and the growth curve of the head provide important clues into making a differentiation between craniosynostosis, primary microcephaly and hydrocephalus.<ref name="Pansynostosis"/> This differentiation has an important influence on the further treatment of the child.<ref name="Pansynostosis"/>

In a recent article Cunningham et al.<ref name="cunningham"/> described several steps in which a pediatrician should observe the patient to assess skull deformity:

• The first is looking with a bird's eye view at the patient while the patient preferably faces the parent while sitting on the parent's lap. The goal is to assess the shape of the forehead, the skull length, the width of the skull, position of the ears and the symmetry of the frontal bones and [occiput].
• The second is looking at the patient from behind while preferably the child is in the same position as described above. It is important to look at the skull base (to determine whether it is level or not), the position of the ears and to the mastoid (to spot the possible presence of a bulge).
• The third point of view is the frontal view. The points to look at are: eye position, eye symmetry and twisting of the nasal tip.

The implications of the deformities that are seen are extensively discussed under 'phenotype'.

Syndromal craniosynostosis presents with a skull deformity as well as deformities affecting other parts of the body.<ref name="Management of craniosynostosis"/> Clinical examination should in any case include evaluation of the neck, spine, digits and toes.<ref name="Management of craniosynostosis"/>

Medical imaging

Radiographic analysis by performing a computed axial tomographic scan is the gold standard for diagnosing craniosynostosis.<ref name="Cerovac">Template:Cite journal</ref><ref name="Goldstein">Template:Cite journal</ref>

Plain radiography of the skull may be sufficient for diagnosing a single suture craniosynostosis and should therefore be performed,<ref name="Cerovac"/><ref name="Goldstein"/> but the diagnostic value is outweighed by that of the CT-scan.<ref name="Aviv">Template:Cite journal</ref> Not only can the sutures be identified more accurately, thus objectively demonstrating a fused suture, but also evaluation of the brain for structural abnormalities and excluding other causes of asymmetric growth are possible at the same time.<ref name="Aviv"/> In addition to this, CT-scanning can visualize the extent of skull deformity, thereby enabling the surgeon to start planning surgical reconstruction.<ref name="Ghali">Template:Cite journal</ref>

Classification

There are several ways to classify craniosynostosis.

• For example, one can consider the number of closed sutures. If only one of the four sutures is prematurely closed (single suture craniosynostosis), the craniosynostosis is referred to as 'simple' (or 'isolated'). Whereas when two or more sutures are no longer open, the craniosynostosis is 'complex'.<ref name="genetics"/>
• A second classification scheme gives a clinical description of the resulting shape of the skull. This will be further discussed under phenotype.
• A third classification involves the presence or absence of an identified craniofacial syndrome. Craniosynostosis where no extracranial deformations are present, is called non-syndromic or 'isolated' craniosynostosis.<ref name="genetics"/> When there are extracranial deformations present, for instance involving the limbs, heart, central nervous system or the respiratory tract,<ref name="cunningham"/> you may speak of a syndromic form of craniosynostosis. More than 180 identified syndromes show deformations due to craniosynostosis.<ref name="genetics"/> The following syndromes are associated with fibroblast growth factor receptors:

Name of syndrome	Other signs and symptoms (along with craniosynostosis; may not all be present)	OMIM reference	Gene
Crouzon syndrome	wide-set, bulging eyes • beaked nose • flat face	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 123500	FGFR2, FGFR3
Apert syndrome	fused fingers or toes • flat midface	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 101200	FGFR2
Crouzonodermoskeletal syndrome	wide-set, bulging eyes • beaked nose • flat face • dark, velvety skin folds • spine abnormalities • benign growths in the jaw	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 134934	FGFR3
Jackson–Weiss syndrome	enlarged, bent big toes • flat midface	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 123150	FGFR1, FGFR2
Muenke syndrome	coronal synostosis • skeletal abnormalities of the hands or feet • hearing loss	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 602849	FGFR3
Pfeiffer syndrome	broad, short thumbs or big toes • webbed or fused fingers or toes	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 101600	FGFR1, FGFR2

In addition, the following syndromes have been identified:

Name of syndrome	Other signs and symptoms (along with craniosynostosis; may not all be present)	OMIM reference	Gene
Loeys–Dietz syndrome	wide-set eyes • split uvula or cleft palate • arterial tortuosity • aortic root dilatation • aneurysms	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 609192 {{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 610168 {{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 613795 {{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 608967 {{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 610380	TGFBR1, TGFBR2, SMAD3
Saethre–Chotzen syndrome	facial asymmetry • low frontal hairline • drooping eyelids • webbed fingers or toes • broad big toes	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 101400	TWIST1
Shprintzen–Goldberg syndrome	bulging eyes • flat face • hernias • long, thin fingers • Developmental disability • intellectual disability	{{#ifeq:none|none	{{#switch:none	short = OMIM:	shortlink = OMIM:	plain = Online Mendelian Inheritance in Man:	full	#default = Online Mendelian Inheritance in Man (OMIM):}}}} {{#if: | - }} 182212	FBN1

Differential diagnosis

Deformational plagiocephaly

The main difference between plagiocephaly based on craniosynostosis and deformational plagiocephaly is that there is no suture fusion in the latter one.<ref name="cunningham"/> The malleability of the neonatal skull allows the skull to change shape due to extrinsic forces.<ref name="cunningham"/>

With the tests a pediatrician should perform, as explained above, the difference is quite easy to make.<ref name="cunningham"/> In deformational plagiocephaly the skull does not show a bulging of the mastoid and in these patients the skull base and position of the ears is level, all in contrary with plagiocephaly due to craniosynostosis.<ref name="cunningham"/> Displacement of one ear to the front is characteristic for deformational plagiocephaly.<ref name="cunningham"/>

Primary microcephaly

Primary microcephaly shows a clinical image of craniosynostosis, but due to a different cause. The primary failure is the absence of growth of the brain, rendering the sutures of the cranial vault useless.<ref name="Pansynostosis"/> As a consequence, the sutures close, presenting a pansynostosis like image.<ref name="Pansynostosis"/> A differentiation between these two conditions can be made with a computed tomography (CT) scan. The subarachnoid spaces are typically enlarged with primary microcephaly, whereas they are reduced or absent in true pansynostosis.<ref name="Pansynostosis"/>

Treatment

The primary goal of surgical intervention is to allow normal cranial vault development to occur.<ref name="Management of craniosynostosis"/> This can be achieved by excision of the prematurely fused suture and correction of the associated skull deformities.<ref name="Management of craniosynostosis"/> If the synostosis goes uncorrected, the deformity will progressively worsen not only threatening the aesthetic aspect, but also the functional aspect.<ref name="Management of craniosynostosis"/> This is especially prevalent with asymmetric conditions, such as unilateral coronal synostosis, with compromised function of the eyes and the jaw.<ref name="Management of craniosynostosis"/> In addition, signs of compromised neurodevelopment have been seen amongst all the synostoses, although this may also be caused by primary maldevelopment of the brain and can thus not be prevented by surgical intervention.<ref name="Spetlz">Template:Cite journal</ref>

There are a few basic elements involved in surgical intervention which is aimed at normalization of the cranial vault:

• Surgery for craniosynostosis is often associated with significant perioperative hemorrhage so multiple strategies are often used to minimize blood loss.<ref>Template:Cite journal</ref> One such method involves the injection of vasoconstrictive agents (i.e. epinephrine) seven to ten minutes before scalp incision.<ref name="Management of craniosynostosis"/> Additionally, the initiation of surgery should be delayed until blood products are physically present in the operating room.<ref name="Management of craniosynostosis"/>
• Another general agreement is the avoidance of the use of titanium plates in the fixation of the skull.<ref name="Fearon">Template:Cite journal</ref><ref name="Duke">

Template:Cite journal</ref> One potential complication following this procedure involves the gradual movement of the titanium plates towards the brain, induced by resorption of the innermost bone layer of the skull with deposition of new bone on the outermost layer, thereby integrating the titanium plates.<ref name="Fearon"/><ref name="Duke"/> In some cases, the plates have been observed to come into direct contact with the brain.<ref name="Fearon"/><ref name="Duke"/> Absorbable plates are now used instead.<ref name="Fearon"/><ref name="Duke"/>

Timing of surgery

The prevention of post-surgical complications, including those mentioned above, plays an important role in discussions over the timing of potential surgery. The general consensus is to perform surgery in late infancy, i.e. between six and twelve months.<ref name="Management of craniosynostosis"/> Within this time frame the efficacy of surgery will be enhanced for several reasons:

• The bone is still more malleable and can be remodelled relatively 'simply' by greenstick fractures of the bone.<ref name="Management of craniosynostosis"/> At approximately one year of age the bone has become more mineralized and brittle and needs to be attached to the surrounding bone with sutures or an absorbable plate.<ref name="Management of craniosynostosis"/>
• Reshaping of the cranial vault most commonly means excision of the bones to allow shape adjustment.<ref name="Management of craniosynostosis"/> Replacement of cranial bones can leave 'gaps' which are readily re-ossified before the age of one year, but will need bony filling thereafter.<ref name="Management of craniosynostosis"/>

Most surgeons will not intervene until after the age of six months due to the heightened risk which blood loss poses before this age.<ref name="Management of craniosynostosis"/> It is generally preferable to wait until after three months of age when anaesthetic risks will also be decreased.<ref name="Management of craniosynostosis"/>

Surgery is not performed in early childhood in every country; in some countries surgical intervention can take place in the late teens.Template:Citation needed

It is important that families seek out a Pediatric Craniofacial Physician who has experience with craniosynostosis for proper diagnosis, surgical care, and followup.

Specific sutures

Sagittal craniosynostosis/scaphocephaly

There are two surgical procedures which are commonly used to treat sagittal synostosis.<ref name="Management of craniosynostosis"/> The matter of which procedure is superior is still heavily debated amongst the surgeons treating this condition,<ref name="Management of craniosynostosis"/> however it is generally agreed upon that the cephalic index should be used to assess the efficacy of the preferred surgical intervention.<ref name="Management of craniosynostosis"/>

• Firstly, the extended strip craniectomy will be discussed, which is a further developed form of the traditional craniectomy.<ref name="Management of craniosynostosis"/> The traditional procedure involved only the excision of the closed suture, with the intent that the compensatory skull deformations would automatically be corrected by the fast growth of the brain during the first year of life.<ref name="Management of craniosynostosis"/>
  This did not quite result in a true normalization of the cranial vault, causing the development of numerous modifications.<ref name="Jimenez">Template:Cite journal</ref><ref name="Baronez">Template:Cite journal</ref> One of those is the extended strip craniectomy. This procedure can be performed by using an endoscope, becoming more popular due to the resultant rapid recovery of the child and reduced need for blood transfusion.<ref name="Jimenez"/><ref name="Baronez"/> The patient is afterwards placed in a custom made molding helmet to correct the resting deformities of the skull.<ref name="Jimenez"/><ref name="Baronez"/>
• In the other widely used surgical procedure, total cranial vault remodelling, the compensatory deformities are corrected during the operation, with excision of the fused suture.<ref name="Francel">Template:Cite book</ref> Most of the bones that collectively form the cranial vault – i.e. the frontal, the parietal and the occipital bones – are removed and reshaped to normalize the contours.<ref name="Francel"/> The bones are then replaced and fixated to form a cranial vault with a normalized shape.<ref name="Francel"/>

Retrospective analysis has given an indication that the use of total cranial vault remodelling provides children with a better cephalic index than does the extended strip craniectomy.<ref name="Panchal J">Template:Cite journal</ref>

An approach that is currently being evaluated involves the use of springs. This intervention is likely most effective when used in the time frame between three and six months of age.

Metopic synostosis/trigonocephaly

The main elements of metopic suture closure involve a low volume of the anterior cranial fossa, the metopic ridging and hypotelorism.<ref name="Metopic synostosis">Template:Cite book</ref> These problems are all addressed during the surgical intervention.<ref name="Metopic synostosis"/>

The volume is increased by placing the frontal bones and the supraorbital rim further forward.<ref name="Management of craniosynostosis"/> This is done by excision of the bones after which they are reshaped with greenstick fracturing.<ref name="Management of craniosynostosis"/> Replacement of the bones provides a possibility for the correction of the hypotelorism at the same time.<ref name="Management of craniosynostosis"/> A bone graft is placed in between the two halves of the supraorbital bars, thereby increasing the width between the orbits.<ref name="Management of craniosynostosis"/> The metopic ridge can then be corrected with a (simple) burring.<ref name="Persing et al"/>

Unilateral coronal synostosis/anterior plagiocephaly

The treatment of unilateral coronal synostosis is typically performed in two parts: the forward advancement of the supraorbital bar and the correction of the orbital asymmetry.<ref name="Management of craniosynostosis"/>

The supraorbital bar is the rim just above the eye socket; as discussed under phenotype, the supraorbital and the frontal bone are typically recessed at the ipsilateral side of the head.<ref name="Management of craniosynostosis"/> The goal of treatment is to position this bar together with the frontal bone in a plane three millimetres further forwards than the vertical plane of the cornea.<ref name="Management of craniosynostosis"/> A two-dimensional sagittal image is used to pre-operatively determine the extent of movement, which can vary between seven and fifteen millimetres depending on the severity of the deformity.<ref name="Management of craniosynostosis"/>

The orbital asymmetry exists typically of a narrower and taller orbit at the ipsilateral side of the head.<ref name="Management of craniosynostosis"/> The contralateral orbit, however, is wider than usual.<ref name="Management of craniosynostosis"/> Symmetry is restored by extracting a small piece of bone from the supraorbital bar at the contralateral side, thereby reducing the width.<ref name="Management of craniosynostosis"/> This bone fragment is then introduced into the supraorbital bar on the ipsilateral side, thereby increasing width.<ref name="Management of craniosynostosis"/> The height of the orbit is altered at the ipsilateral side only, by extracting a piece of bone.<ref name="Management of craniosynostosis"/> Any correction of the nasal tip, which points towards the contralateral side, will not be performed during childhood.<ref name="Persing et al"/>

Unilateral lambdoid synostosis/posterior plagiocephaly

An excision of the flattened occipital bone with release of the fused suture tends to correct the cranial vault deformity.<ref name="Persing et al"/>

Bilateral coronal synostosis/brachycephaly

The treatment of bilateral coronal synostosis shows a high degree of overlap with treatment of unilateral coronal synostosis; in both surgical interventions is the forward advancement of the supraorbital rim together with the frontal bones is an important part of the procedure.<ref name="Persing et al"/><ref name="Management of craniosynostosis"/> Again, the plane three millimetres further forwards than the vertical plane of the [cornea] is the appropriate position to place the bone.<ref name="Persing et al"/><ref name="Management of craniosynostosis"/> The increased height of the skull is addressed in the same procedure.<ref name="Persing et al"/> Parts of the flattened occiput are extracted and given a rounder shape by greenstick fracturing them.<ref name="Persing et al"/>

Pansynostosis/kleeblattschädel

The treatment of pansynostosis comprises the expansion of the anterior cranial vault, as well as the posterior cranial vault.<ref name="Pansynostosis"/> Whilst this may be accomplished in one procedure it is generally performed in two stages.<ref name="Pansynostosis"/>

Complications

The most common complications of uncorrected craniosynostosis include increased intracranial pressure, asymmetry of the face, and malocclusion. Asymmetry of the orbits often leads to strabismus.<ref name="pmid15222651">Template:Cite journal</ref>

Epidemiology

It is estimated that craniosynostosis affects 1 in 1,800 to 3,000 live births worldwide.<ref name="Brief Review"/> three out of every four cases affect males. Sagittal synostosis is the most common phenotype, representing 40% to 55% of nonsyndromic cases,<ref name="Brief Review"/> whilst coronal synostosis represents between 20% and 25% of cases.<ref name="Brief Review"/> Metopic synostosis is a factor in 5% to 15% of cases, and lambdoid synostosis is seen in 0% to 5% of nonsyndromic cases.<ref name="Brief Review"/>

Five to 15% of the time more than one suture is involved; this is referred to as "complex craniosynostosis" and is typically part of a syndrome.<ref name="Brief Review"/>

External links

• GeneReview/NIH/UW entry on FGFR-Related Craniosynostosis Syndromes
• Template:Cite journal