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Up to: DNA repair disease · Ataxia-telangiectasia-like disorder
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
A rare autosomal recessive cerebellar ataxia (ARCA), characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.
This condition has no sub-types.