Catalog
Spinocerebellar ataxia
Link to WHO Definition
Spinocerebellar ataxia – http://id.who.int/icd/entity/600993818
Autosomal dominantly inherited ataxias associated with over 37 gene loci that involve progressive degeneration of the cerebellum and spinocerebellar tracts of the spinal cord, presenting with characteristic sensory loss, diminished tendon reflexes, Romberg sign, and positive Babinski sign(s).