Spinocerebellar ataxia (Q41029): Difference between revisions
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Revision as of 07:04, 13 August 2026
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).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A03.16 |
||
| English | Spinocerebellar ataxia |
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). |
