Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

A rare autosomal recessive cerebellar ataxia (ARCA), characterized by progressive cerebellar ataxia associated with frequent oculomotor apraxia, severe neuropathy and an elevated serum alpha-fetoprotein (AFP) level.

Also known as: AOA2, SCAN 2, SCAN2, ataxia with oculomotor apraxia type 2, ataxia-ocular apraxia 2, ataxia-oculomotor apraxia 2, ataxia-oculomotor apraxia type 2, spinocerebellar ataxia with axonal neuropathy type 2

29 clinical trials for this condition and its sub-types.