Pyruvate dehydrogenase complex E2 subunit deficiency (Q83521): Difference between revisions

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A deficiência de piruvato desidrogenase E2 é uma forma muito rara de deficiência de piruvato desidrogenase (PDHD), caracterizada por acidose láctica variável e disfunção neurológica, que aparece principalmente durante a infância.
description / endescription / en
 
Pyruvate dehydrogenase E2 deficiency is a very rare form of pyruvate dehydrogenase deficiency (PDHD, ) characterised by variable lactic acidosis and neurological dysfunction, mainly appearing during childhood.
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Property / Canonical URI: https://id.who.int/icd/entity/1626957624 / rank
 
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CID11:ID_1626957624
Property / CURIE: CID11:ID_1626957624 / rank
 
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dki-india-ID_1626957624
Property / Canary Token: dki-india-ID_1626957624 / 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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CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 08:53, 15 August 2026

Pyruvate dehydrogenase E2 deficiency is a very rare form of pyruvate dehydrogenase deficiency (PDHD, ) characterised by variable lactic acidosis and neurological dysfunction, mainly appearing during childhood.
Language Label Description Also known as
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ID_1626957624
    English
    Pyruvate dehydrogenase complex E2 subunit deficiency
    Pyruvate dehydrogenase E2 deficiency is a very rare form of pyruvate dehydrogenase deficiency (PDHD, ) characterised by variable lactic acidosis and neurological dysfunction, mainly appearing during childhood.

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      CID11:ID_1626957624
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      dki-india-ID_1626957624
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      Concluído
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      13 August 2026
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