Wilson disease (WD) is a potentially treatable, inherited disorder of copper metabolism that is characterized by the pathological accumulation of copper. WD is caused by mutations in ATP7B, which encodes a transmembrane copper-transporting ATPase, leading to impaired copper homeostasis and copper overload in the liver, brain and other organs.

Negligence towards health gives rise to many diseases, while there are some diseases that a person gets through his parents, which are called genetic diseases. One such disease is Wilson’s disease.

You may have heard this name for the first time, but it is important to be aware of it so that its effect can be reduced in time. That is why in this article of Myhealthonly, we have shared information related to the causes, symptoms, and treatment of Wilson’s disease.