a rare hereditary disease in which copper accumulates in the brain and liver, gradually leading to tremors, muscular rigidity, kidney malfunction, and cognitive disturbances: marked by Kayser-Fleischer rings.
Origin of Wilson's disease
named after Samuel Alexander Kinnier Wilson (1878–1936), British neurologist, who described it in 1912
An inherited disorder of copper metabolism characterized by cirrhosis, degeneration of the basal ganglia of the brain, and the deposition of green pigment in the periphery of the cornea.hepatolenticular degeneration
