Maternally inherited Leigh syndrome (Q89272): Difference between revisions
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A Síndrome de Leigh de herança materna é um subtipo raro da síndrome de Leigh caracterizada clinicamente por encefalopatia, acidose láctica, convulsões, cardiomiopatia, distúrbios respiratórios e atraso no desenvolvimento, com início na primeira infância e resultante de mutações herdadas do DNA mitocondrial materno. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
