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Autosomal Recessive Spinocerebellar Ataxia 13
An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that is caused by homozygous mutation in the GRM1 gene on chromosome 6q24.
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When to seek help
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Overview
An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that is caused by homozygous mutation in the GRM1 gene on chromosome 6q24.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.