Wilson's disease is a rare genetic disorder that leads to the excessive accumulation of copper in the body, particularly in the liver and brain. It is caused by mutations in the ATP7B gene, which impairs the body's ability to excrete copper through bile, resulting in toxic levels that can cause serious health problems. The prevalence of Wilson's disease is estimated to be about 1 in 30,000 individuals in the general population, and it affects both males and females equally. If not diagnosed and treated, the condition can lead to severe liver disease, neurological impairments, and even death; however, early detection and appropriate treatment can significantly improve outcomes. Treatments typically include lifelong use of chelating agents, such as penicillamine, which help remove excess copper from the body, highlighting the importance of awareness and understanding of this genetic condition.
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