Maternally-inherited Leigh syndrome

Maternally 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.

Also known as: MILS, maternally-inherited Leigh disease, maternally-inherited infantile subacute necrotizing encephalopathy, Leigh disease, maternally inherited, Subacute necrotizing encephalomyelopathy maternally inherited, maternally inherited Leigh syndrome, mitochondrial DNA-associated Leigh syndrome

19 clinical trials for this condition and its sub-types, 1 tagged with Maternally-inherited Leigh syndrome itself.