Caused by disease
Is a mutated body disorder, where there is a mutation in a specific gene located on chromosome 13, has been identified more than 300 gene mutation, and there is a failure to collect copper with the core of serylobulazmin leading to low serioloplasmin, and there is also a shortage of copper secretion In addition, the absorption of copper from the small intestine leads to the accumulation of copper in various organs of the body, especially the liver, brain and cornea, and the disease affects 1 in every 30,000 to 100,000 people, and particularly affects the Caucasians It is rare in Indians and Asians, and is limited Wilson disease in all countries of the world, especially countries where the marriage of relatives is widespread.