Wilson disease is associated with abnormal metabolism of
A
Iron
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B
Potassium
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C
Copper
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D
Iodine
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Solution
The correct option is B Copper
Wilson disease is a rare autosomal recessive inherited disorder of copper metabolism that is characterized by excessive deposition of copper in the liver, brain, and other tissues. Wilson disease is caused by mutations in the ATP7B gene. This gene provides instructions for making a protein called copper-transporting ATPase 2, which plays a role in the transport of copper from the liver to other parts of the body.