Autosomal recessive spastic ataxia 4
Alternate names[edit | edit source]
SPAX4; Spastic ataxia 4, autosomal recessive; Autosomal recessive spastic ataxia - optic atrophy - dysarthria; Autosomal recessive spastic ataxia type 4; Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome
Definition[edit | edit source]
A rare, genetic, autosomal recessive spastic ataxia disease characterized by onset in early childhood of spastic paraparesis, cerebellar ataxia, dysarthria and optic atrophy.
NIH genetic and rare disease info[edit source]
Autosomal recessive spastic ataxia 4 is a rare disease.
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