Spinocerebellar ataxia (Q41029)

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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).
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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).

      Statements

      CID11:8A03.16
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      dki-india-8A03.16
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      Concluído
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      13 August 2026
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