Spinocerebellar ataxia type 36 (Q101105): Difference between revisions

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15 August 2026
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Latest revision as of 17:54, 16 August 2026

Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasciculations, tongue atrophy and hyperreflexia.
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ID_1544814018
    English
    Spinocerebellar ataxia type 36
    Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasciculations, tongue atrophy and hyperreflexia.

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      CID11:ID_1544814018
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      dki-india-ID_1544814018
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      Concluído
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      15 August 2026
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