An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.
synonyms:
OMIM:616719,
autosomal recessive spinocerebellar ataxia 21 with hepatopathy,
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome,
