دورة تعليم مستمر في العلوم الأساسية السادسة

8 May 2022, 09:00 → 13 May 2022, 11:00 Asia/Baghdad

كلية طب الاسنان

ا.م.د. وفاء منصور ميرزا, ا.م.رشا عباس عزيز , ا.م.شيماء سبتي , ا.م.هبة فاضل, م.زينب غالب

Wilson disease is a rare genetic disorder characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes. The disease is progressive and, if left untreated, it may cause liver (hepatic) disease, central nervous system dysfunction, and death. What causes Wilson disease? Mutations link of a gene called ATP7B cause Wilson disease. These gene mutations prevent the body from removing extra copper. Normally, the liver releases extra copper into bile.

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biochemical features of wilson disease1.pdf

histology of wilson disease.pdf

treatment of wilson disease.pdf

Wilson Disease.pdf

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