Idiopathic copper-associated cirrhosis

Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.

Also known as: non-Wilsonian hepatic copper toxicosis of infancy and childhood

0 clinical trials for this condition and its sub-types, 0 tagged with Idiopathic copper-associated cirrhosis itself.