Richards-Rundle syndrome (Q60243): Difference between revisions

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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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CalendarGregorian
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Latest revision as of 07:45, 14 August 2026

Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.
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ID_114583632
    English
    Richards-Rundle syndrome
    Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.

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      CID11:ID_114583632
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      dki-india-ID_114583632
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      Concluído
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      13 August 2026
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