Catalog

Autosomal recessive ataxia with oculomotor apraxia type 2

No MMS code

Link to WHO Definition

Autosomal recessive ataxia with oculomotor apraxia type 2 – http://id.who.int/icd/entity/907196820

Ataxia-oculomotor apraxia type 2 is a form of autosomal recessive cerebellar ataxia characterised by progressive cerebellar ataxia, axonal sensorimotor neuropathy with oculomotor apraxia, fixation instability, extrapyramidal features and an elevated serum alpha-fetoprotein level.