Not known Details About maladie de wilson
Not known Details About maladie de wilson
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Stage 2: There's a redistribution of copper within the liver cells and then the excess thus spills into the bloodstream
Wilson's disease is brought on by a mutation within the Wilson disease protein (ATP7B) gene. This protein transports extra copper into bile, where by it really is excreted in waste products. The affliction is autosomal recessive; for men and women to get affected, they need to inherit a mutated copy in the gene from both mom and dad.
The excess copper can build up from the liver and/or brain triggering liver destruction and/or neurological complications. It can also gather in other areas of your body such as the eyes and also the kidneys.
Des problems neurologiques peuvent s'observer en second lieu. C'est lorsque le cuivre s’accumule dans le cerveau et perturbe son fonctionnement. On parle notamment de :
Progressive lenticular degeneratio. A familial anxious disease affiliated with cirrhosis from the liver.
Une greffe de foie peut guérir la maladie et peut sauver la vie des personnes atteintes par la maladie de Wilson et souffrant d’insuffisance hépatique ou de problèmes hépatiques graves qui ne répondent pas au traitement médicamenteux.
De réduire au optimum les apports en cuivre dans l’alimentation du chien et de favoriser l’excrétion du cuivre.
Wilson disease is assessed less than autosomal recessive ailment. Because of this anyone can only get this condition when there is an inheritance of two irregular ATP7B genes, 1 from both equally dad and mom (I.e. a person from your mom and another from The daddy).
Il existe un traitement efficace pour lutter contre cette maladie. Cependant, le diagnostic précoce de cette maladie pose un problème, automobile la maladie de Wilson ne se détecte pas facilement et reste longtemps silencieuse.
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There are many hereditary diseases that bring about copper overload in the liver; more info Wilson's disease is the most common of them. All can cause cirrhosis at a younger age. Another copper overload diseases are Indian childhood cirrhosis (ICC), endemic Tyrolean infantile cirrhosis, and idiopathic copper toxicosis.
La maladie de Wilson est une pathologie génétique unusual qui est liée à une accumulation de cuivre dans l'organisme et as well as particulièrement dans le foie et le cerveau.
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