Pyruvate dehydrogenase complex E3 subunit deficiency (Q83528): Difference between revisions
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A deficiência de piruvato desidrogenase E3 é um subtipo muito raro de deficiência de piruvato desidrogenase (PDHD), caracterizada por acidose láctica de início precoce e atraso do desenvolvimento, disfunção neurológica de início tardio ou doença hepática. | |||
| description / en | description / en | ||
Pyruvate dehydrogenase E3 deficiency is a very rare subtype of pyruvate dehydrogenase deficiency (PDHD, ) characterised by either early-onset lactic acidosis and delayed development, later-onset neurological dysfunction or liver disease. | |||
Revision as of 08:53, 15 August 2026
Pyruvate dehydrogenase E3 deficiency is a very rare subtype of pyruvate dehydrogenase deficiency (PDHD, ) characterised by either early-onset lactic acidosis and delayed development, later-onset neurological dysfunction or liver disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1948020523 |
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| English | Pyruvate dehydrogenase complex E3 subunit deficiency |
Pyruvate dehydrogenase E3 deficiency is a very rare subtype of pyruvate dehydrogenase deficiency (PDHD, ) characterised by either early-onset lactic acidosis and delayed development, later-onset neurological dysfunction or liver disease. |
