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Medicine General a27b1793

True about Wilson’s disease

A
Decreased urinary excretion of copper
B
Increased ceruloplasmin in blood
C
Decreased copper and ceruloplasmin in serum
D
Decreased urinary excretion of ceruloplasmin
High-Yield Explanation
In Wilson’s disease, there is almost always a failure of synthesis of ceruloplasmin; however, some 5% of patients have a normal circulating ceruloplasmin concentration and this is not the primary pathogenic defect. The amount of copper in the body at birth is normal but thereafter it increases steadily; the organs most affected are the liver, basal ganglia of the brain, eyes, kidneys and skeleton.

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