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Maternally-inherited Leigh syndrome
rareMaternally inherited Leigh syndrome is a rare subtype of Leigh syndrome characterized 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.
- Identifiers
- MONDO:0016814 Orphanet:255210
- Part of
- Leigh syndrome
- Also known as
- Leigh disease, maternally inherited · maternally inherited Leigh syndrome · maternally-inherited infantile subacute necrotizing encephalopathy · maternally-inherited Leigh disease · MILS
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