Wilson's Disease: Causes, Symptoms and Treatment

Wilson’s disease sponsored by Wilson’s disease is a genetic defect caused by copper collection in the tissues of certain organs of the body, such as: the liver, kidneys, brain and eye cornea, which do serious damage. Symptoms of Wilson’s disease When you talk about the symptoms of Wilson’s disease are as follows: 1 symptoms of a disease in a liver that forms a primary sign of this disease that occurs in about half of the patients, especially the occurrence of liver cirrhosis, and the defect in the performance of the liver. In a smaller part of 10% – 30% of patients, chronic liver inflammation arises in the liver, and in rare cases, Wilson’s disease is also discovered, due to severe liver and sudden liver failure and severe high levels of bilirubin in the blood that are constantly rising. 2. Neurological symptoms can begin with different motor disorders, such as: involuntary movements. Throw and compromise. Inertia in motion and speech … unstable step. Stutter. Inability to relax. 3.. Psychological symptoms, the most prominent: large and early decline in spiritual abilities. Changes in the personality and unstable behavior. Reduced academic achievement. The rise of strange behavior. Symptoms of schizophrenia -symptoms occur. Causes and factors of the risk of Wilson disease cause the disease of a dysfunction in the 13 (13 (chromosome) genes to produce an adenosine triphosphatase – ATPase – which works in the body as a copper container. Wilson’s disease. A circulating and acceptable disease: 1. Penicillamine, which is linked to copper and causes it to get rid of large amounts of it in the urine, reducing its deposition into the important organs in the body. 2.. Prevention of Wilson’s disease There is no way to prevent disease.