Catalog

X-linked spinocerebellar ataxia type 3

No MMS code

Link to WHO Definition

X-linked spinocerebellar ataxia type 3 – http://id.who.int/icd/entity/261426817

X-linked spinocerebellar ataxia type 3 is a form of spinocerebellar degeneration characterised by onset in infancy of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropia, and optic atrophy, and by a progressive course leading to death in childhood.

Parents