Spinocerebellar ataxia type 22 (Q101080)

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Spinocerebellar ataxia type 22 (SCA22) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar ataxia and hyporeflexia.
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ID_1835077432
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    Spinocerebellar ataxia type 22
    Spinocerebellar ataxia type 22 (SCA22) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar ataxia and hyporeflexia.

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      CID11:ID_1835077432
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      dki-india-ID_1835077432
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      Concluído
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      15 August 2026
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