Hereditary Coproporphyria (HCP): Symptoms, Causes
Hereditary coproporphyria (HCP) is a rare genetic disorder characterized by a deficiency in the enzyme coproporphyrinogen oxidase (CPOX), which is crucial in the heme biosynthesis pathway. This condition is classified as an acute hepatic porphyria, manifesting with intermittent neurovisceral attacks. Causes of Hereditary Coproporphyria HCP is caused by mutations in the CPOX gene. This gene