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"WILSON DISEASE"

This is a rare, autosomal recessive disorder of copper metabolism . Copper accumulates in the liver initially ; once the liver is saturated,...

This is a rare, autosomal recessive disorder of copper metabolism. Copper accumulates in the liver initially; once the liver is saturated, copper deposition occurs in the basal ganglia, renal tubules, cornea (Kayser-Fleischer rings), bones, joints and parathyroid glands.
US

•  Imaging features are non-specific.
•   Fatty infiltration.
•  Acute or chronic hepatitis.
•  Cirrhosis or liver necrosis.

MRI

•  Cirrhosis.
•  Findings are non-specific.