Autosomal recessive spastic ataxia of Charlevoix-Saguenay

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Name:
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Description:
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterised by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy.
ORPHAcode:
98
Synonyms:
ARSACS
Autosomal recessive spastic ataxia type 6
SPAX6
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14