Hepatolenticular Degeneration
Quick Boards Review: Hepatolenticular Degeneration Wilson’s Disease, also known as Hepatolenticular Degeneration, is a rare, autosomal recessive mutation in the ATP7B gene.1 This mutation causes a decrease in serum ceruloplasmin which is an important chaperone protein that aids in removing copper in the body.2 This is detrimental because when copper is not removed from the body, it …