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 / en | description / 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. | |||
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 |
|---|---|---|---|
| default for all languages | ID_1626957624 |
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| 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. |
