Spinocerebellar ataxia with axonal neuropathy type 2

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Name:
Spinocerebellar ataxia with axonal neuropathy type 2
Description:
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.
ORPHAcode:
64753
Synonyms:
AOA2
Ataxia-oculomotor apraxia type 2
SCAN 2
SCAR1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14