Wilson's Disease
Wilson's Disease is a rare genetic disorder that causes excessive copper accumulation in the body, particularly in the liver and brain. Normally, the body removes excess copper, but in Wilson's Disease, this process is disrupted due to a faulty gene. As copper builds up, it can lead to serious health issues, including liver damage, neurological problems, and psychiatric symptoms. Early diagnosis and treatment, often involving medication to remove excess copper, are crucial to manage the disease and prevent complications. Regular monitoring and a diet low in copper can also help those affected lead healthier lives.
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Wilson's disease is a genetic disorder that prevents the body from properly eliminating copper, leading to its accumulation in the liver, brain, and other organs. This buildup can cause various symptoms, including liver disease, neurological issues, and psychological problems. It usually begins in childhood or young adulthood and can be diagnosed through blood tests, a liver biopsy, or genetic testing. Treatment often involves medications to remove excess copper and dietary changes to reduce copper intake. Early diagnosis and management are crucial to prevent serious complications.