Catalog
Autosomal dominant cerebellar ataxia type 3
No MMS code
Link to WHO Definition
Autosomal dominant cerebellar ataxia type 3 – http://id.who.int/icd/entity/390406504
Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.
Parents
Children
- Spinocerebellar ataxia type 6
- Spinocerebellar ataxia type 10
- Spinocerebellar ataxia type 31
- Spinocerebellar ataxia type 29
- Spinocerebellar ataxia type 15
- Spinocerebellar ataxia type 26
- Spinocerebellar ataxia type 30
- Spinocerebellar ataxia type 14
- Spinocerebellar ataxia type 11
- Spinocerebellar ataxia type 5
- Spinocerebellar ataxia type 25
- Spinocerebellar ataxia type 20