Conditions / Genetic
cytochrome-c oxidase deficiency disease
info ยท Genetic
A mitochondrial metabolism disease that is characterized by deficiency of cytochrome c oxidase, myopathy, hepatomegaly, hypertrophic cardiomyopathy, lactic acidosis, and Leigh syndrome, and is caused by mutations related to oxidative phosphorylation.
Also known as: MITOCHONDRIAL COMPLEX IV DEFICIENCY