Editing Plagiocephaly (section)

=== Conditions and syndromes ===
Plagiocephaly is seen in multiple conditions:<ref>{{Cite web |title=Plagiocephaly[Clinical Features] - MedGen - NCBI |url=https://www.ncbi.nlm.nih.gov/medgen?term=Plagiocephaly%5BClinical+Features%5D&cmd=DetailsSearch |access-date=2023-10-29 |website=www.ncbi.nlm.nih.gov}}</ref>
* [[Arthrogryposis]], [[Cleft lip and cleft palate|cleft palate]], craniosynostosis, and impaired [[Cognitive development|intellectual development]]
* [[Autism spectrum disorder]], susceptibility to, X-linked 2
* [[Blepharophimosis intellectual disability syndromes|Blepharophimosis-impaired intellectual development syndrome]]
* Cardiac anomalies - [[Global developmental delay|developmental delay]] - [[Dysmorphic feature|facial dysmorphism]] syndrome
* [[CHIME syndrome]]
* [[Coffin–Siris syndrome|Coffin-Siris syndrome]] 1 and 6
* [[Congenital myopathy|Congenital nonprogressive myopathy]] with [[Moebius syndrome|Moebius]] and [[Pierre Robin sequence|Robin sequences]]
* [[Cornelia de Lange syndrome]] 3
* [[Sensenbrenner syndrome|Cranioectodermal dysplasia]] 2
* Craniosynostosis (nonsyndromic) 6
* Developmental and epileptic [[encephalopathy]], 1, 65, 77, and 84
* Developmental delay with variable [[Developmental disability|intellectual impairment]] and [[Abnormality (behavior)|behavioral abnormalities]]
* [[Dihydropyrimidinase]] deficiency
* Early-onset progressive diffuse [[Cerebral atrophy|brain atrophy]]-[[microcephaly]]-[[muscle weakness]]-[[Optic neuropathy|optic atrophy]] syndrome
* [[Faciocardiorenal syndrome]]
* [[FG syndrome]]
* [[Galloway Mowat syndrome|Galloway-Mowat syndrome]] 4
* [[Conjugate gaze palsy|Gaze palsy]], familial horizontal, with progressive [[scoliosis]] 1
* [[Hyperphosphatasia with mental retardation syndrome|Hyperphosphatasia with intellectual disability syndrome]] 1 and 2
* [[Hypotonia]], infantile, with [[psychomotor retardation]] and [[Facies (medical)|characteristic facies]] 2
* Intellectual developmental disorder, autosomal dominant 64 and 66
* Intellectual disability, autosomal dominant 13, 40, 48, and 58
* [[Joubert syndrome]] 1
* [[9q34.3 deletion syndrome|Kleefstra syndrome]] 2
* [[Langer–Giedion syndrome|Langer-Giedion syndrome]]
* [[Microphthalmia]] with brain and digit anomalies
* [[Mitochondrial DNA depletion syndrome]] 13
* [[Muenke syndrome]]
* [[Noonan syndrome]] 13
* [[Osteogenesis imperfecta]], type 20
* [[3C syndrome|Ritscher-Schinzel syndrome]] 4
[[File:Shuttleworth Potts Plate X (1).jpg|thumb|Plagiocephaly with [[oxycephaly]] in Saethre-Chotzen syndrome]]
* [[Saethre–Chotzen syndrome|Saethre-Chotzen syndrome]]
* [[Hereditary spastic paraplegia|Spastic paraplegia]], intellectual disability, [[nystagmus]], and [[obesity]]
* Syndromic [[X-linked intellectual disability]] Najm type