Wilson's disease is a rare genetic disorder that causes a buildup of copper in the body. This can lead to severe damage to the liver, brain, and other organs. Symptoms often develop gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and ge

La maladie de Wilson est une condition génétique rare qui entraîne un excès d'accumulation de cuivre dans l'organisme. Pour gérer cette accumulation, il est important d'adopter une diète sans cuivre. Il existe plusieurs formules simples et délicieuses que vous pouvez employer pour limiter votre consommation de cuivre tout en rassurant vos be

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Wilson disease affects a rare genetic disorder that causes excessive copper to accumulate in the liver, brain, and other organs. This buildup may serious health problems if left untreated. The condition is inherited mutations in a gene called ATP7B, which regulates copper transport within the body. Symptoms of Wilson disease can be diverse and oft