X-linked sideroblastic anaemia with ataxia (Q85648): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/609727552 / rank
 
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CID11:ID_609727552
Property / CURIE: CID11:ID_609727552 / rank
 
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dki-india-ID_609727552
Property / Canary Token: dki-india-ID_609727552 / rank
 
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 11:00, 15 August 2026

X-linked sideroblastic anaemia with ataxia (XLSA/A) is a hereditary ataxia characterised by motor delay, ataxia evident from early childhood, and dysarthria. Neurological features are non-progressive. Patients usually have a mild asymptomatic anaemia or a borderline decreased mean corpuscular volume.
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ID_609727552
    English
    X-linked sideroblastic anaemia with ataxia
    X-linked sideroblastic anaemia with ataxia (XLSA/A) is a hereditary ataxia characterised by motor delay, ataxia evident from early childhood, and dysarthria. Neurological features are non-progressive. Patients usually have a mild asymptomatic anaemia or a borderline decreased mean corpuscular volume.

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      CID11:ID_609727552
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      dki-india-ID_609727552
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      Concluído
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      13 August 2026
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