Pyruvate dehydrogenase complex deficiency (Q40050)

From determinar.ia.br - Determine suas informações
Revision as of 05:42, 13 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Pyruvate dehydrogenase deficiency (PDHD) is a rare neurometabolic disorder characterised by a wide range of clinical signs with metabolic and neurological components of varying severity. Manifestations range from often fatal, severe, neonatal to later-onset neurological disorders.
Language Label Description Also known as
default for all languages
5C53.02
    English
    Pyruvate dehydrogenase complex deficiency
    Pyruvate dehydrogenase deficiency (PDHD) is a rare neurometabolic disorder characterised by a wide range of clinical signs with metabolic and neurological components of varying severity. Manifestations range from often fatal, severe, neonatal to later-onset neurological disorders.

      Statements

      CID11:5C53.02
      0 references
      dki-india-5C53.02
      0 references
      Concluído
      0 references
      13 August 2026
      0 references
      0 references