Multisystem developmental disorder
Multisystem developmental disorder (MSDD) is a term used by Stanley Greenspan to describe children under age 3 who exhibit signs of impaired communication as in autism, but with strong emotional attachments atypical of autism.Template:Citation needed It is described in the DC:0-3R manual as an optional diagnosis for children under two years of age.<ref>Template:Cite journal</ref><ref name="Oztop 2007">Template:Cite journal</ref>
Other uses of the termEdit
The term multisystem developmental disorder has also been used to describe various developmental disorders. These include:
- Alagille syndrome,<ref name=a>Template:Cite journal</ref> an autosomal dominant disorder with a wide range of features and manifestations. Its five most significant features are chronic cholestasis, a condition where bile cannot flow from the liver to the duodenum, occurring in 95% of cases; heart abnormalities (over 90%); butterfly vertebrae; posterior embryotoxon and a distinctive face (prominent forehead, deep-set eyes, and a pointed chin).<ref>Template:Cite journal</ref>
- Rubinstein-Taybi syndrome,<ref name=rt>Template:Cite journal</ref><ref>{{#invoke:citation/CS1|citation
|CitationClass=web }}</ref> a syndrome characterized by broad thumbs, facial abnormalities, and big toes alongside moderate to severe intellectual disability.<ref>Template:Cite journal</ref>
- Williams syndrome,<ref name=w>Template:Cite journal</ref><ref name=wb>Template:Cite journal</ref> a neurodevelopmental disorder characterized by a unique profile of strengths and deficits; most with the condition have mild intellectual disability but have grammatical and lexical abilities above what would be expected from their IQs.<ref>Template:Cite book</ref> They are hypersocial and empathetic, but social isolation is commonly experienced.<ref>Template:Cite book</ref>
- Proteus syndrome,<ref>Template:Cite journal</ref> a congenital disorder causing disproportionate growth of skin, bone, and other tissues.<ref>Template:Cite journal</ref>
- Asphyxiating thoracic dysplasia,<ref>Template:Cite journal</ref> an autosomal recessive skeletal disorder with an estimated prevalence of between 1 in 100,000 and 1 in 130,000 live births.<ref>Template:Cite journal</ref>
SymptomsEdit
- Toe walking<ref name="Woliver2009">Template:Cite book</ref>
- Pragmatic speech problems<ref name="Woliver2009" />
- Clumsiness<ref name="Woliver2009" />
- Obsessions and rituals<ref name="Woliver2009" />
- Sensory issues<ref name="Woliver2009" />
- Disinterest in social interaction<ref name="Woliver2009" />
- Autistic characteristics<ref name="Woliver2009" />
ReferencesEdit
Further readingEdit
- Template:Cite journal
- Increasing Interaction with Children with Multisystem Developmental Disorder (MSDD), Developmental Delay Resources
- Template:Cite journal