Spinocerebellar ataxia (Q41029): Difference between revisions

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Ataxias hereditárias autossômicas dominantes associadas a mais de 37 locus gênicos que envolvem degeneração progressiva de cerebelo e tratos espinocerebelares da medula espinal, apresentando-se com perda sensitiva característica, reflexos tendinosos diminuídos, sinal de Romberg e sinal(is) de Babinski positivo(s).
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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).

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).
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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).

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