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