Carnitine palmitoyltransferase (CPT) deficiency

Carnitine palmitoyltransferase II (CPT) deficiency is the most common inherited lipid-metabolism disorder in skeletal muscle. Read more »
Mitochondrial myopathy seen on H&E stain, trichrome stain, CO stain

Mitochondrial myopathy

Mitochondrial myopathy can be caused by metabolic abnormalities related to mutations in the mitochondrial genome or mutations in the somatic genome that produce abnormal mitochondrial proteins. Read more »