Wilson's Disease : Symptoms
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Symptoms could include:
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Kayser-Fleischer ring
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Enlargement of the abdomen (abdominal distention; Splenomegaly; Yellow skin (jaundice) or yellow color of the white of the eye (icterus; Vomiting blood; Weakness; Tremors of the arms or hands; Difficulty moving arms and legs, stiffness; Abnormal a...
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Wilson disease is a rare, inherited disorder that causes excess copper to accumulate in the body. Steadily increasing amounts of copper circulating in the blood are deposited primarily in the brain, liver, kidneys, and the cornea of the eyes.
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Wilson disease (WD) is an inherited disorder of copper metabolism, transmitted as an autosomal recessive trait. This type of inheritance means unaffected parents who each carry the WD gene have a 25% risk in each pregnancy of having an affected ch...
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Wilson disease is a rare, inherited disorder that causes excess copper to accumulate in the body. Steadily increasing amounts of copper circulating in the blood are deposited primarily in the brain, liver, kidneys, and the cornea of the eyes.
|
 |
Wilson disease is a rare, inherited disorder that causes excess copper to accumulate in the body. Steadily increasing amounts of copper circulating in the blood are deposited primarily in the brain, liver, kidneys, and the cornea of the eyes.
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