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Dec 2, 2023 · Wilson's disease is a rare inherited condition that causes copper levels to build up in several organs, especially the liver, brain and eyes. Most people with Wilson's disease are diagnosed between the ages of 5 and 35.
Aug 7, 2023 · Wilson disease is an autosomal recessive condition caused by a mutation in the Wilson disease protein (ATP7B) gene. For a person to be affected, a copy of the gene from each parent need to be inherited.
Wilson's disease (also called Hepatolenticular degeneration) is a genetic disorder characterized by the excess build-up of copper in the body. Symptoms are typically related to the brain and liver. Liver-related symptoms include vomiting, weakness, fluid build-up in the abdomen, swelling of the legs, yellowish skin, and itchiness.
Definition & Facts. Wilson disease is a genetic disorder that prevents the body from removing extra copper, causing copper to build up in the liver, brain, eyes, and other organs. Without treatment, high copper levels can cause life-threatening organ damage.
Jul 31, 2023 · Wilson disease (also referred to as hepatolenticular degeneration) is a genetic disorder of copper metabolism with an autosomal recessive pattern of inheritance that leads to impaired function of the intracellular copper transporter ATP7B.
Wilson disease is present at birth, but the symptoms don’t appear until the copper builds up in the liver, the brain, or other organs. Some people do not have symptoms of Wilson disease before they are diagnosed with the disease and treated.
Wilson disease is a rare genetic disorder passed from parents to children (inherited). It prevents your body from getting rid of extra copper in your system. Your body needs small amounts of copper from food to stay healthy. But too much copper is toxic.
Jul 19, 2024 · Wilson disease (WD) is a rare inherited disorder in which an excessive amount of copper accumulates in the body. The buildup of copper leads to damage in the liver, brain, and eyes. Although copper accumulation begins at birth, symptoms of the disorder only appear later in life.
Nov 2, 2023 · Wilson's disease is an autosomal-recessive disease of copper accumulation and toxicity caused by a defect in an enzyme involved in the excretion of excess copper. Estimated prevalence is 1 in 30,000 to 1 in 50,000, with no sex or ethnic predominance.
Wilson disease is a genetic disorder that prevents the body from removing extra copper, causing copper to build up in the liver, brain, eyes, and other organs. Your body needs a small amount of copper from food to stay healthy, but too much copper is harmful.
