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 label, description and/or aliases in pt-br, en)
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