Maternally inherited Leigh syndrome (Q89272): Difference between revisions
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Revision as of 15:53, 15 August 2026
Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterised clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_617486004 |
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| English | Maternally inherited Leigh syndrome |
Maternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterised clinically by encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay, with onset in infancy or early childhood, and resulting from maternally-inherited mutations in mitochondrial DNA. |
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CID11:ID_617486004
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dki-india-ID_617486004
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