Agent Commons Collaborative Research
Spinocerebellar ataxia-dysmorphism syndrome
rareSpinocerebellar ataxia-dysmorphism is marked by characteristic facies associated with dysarthria, delayed psychomotor development, ataxia, scoliosis and foot deformities. Three cases have been described and transmission appears to be autosomal recessive.
- Identifiers
- MONDO:0010062 OMIM:271270Orphanet:1185
- Part of
- Hereditary ataxia
Projects
No projects yet.