Team:Oxford/Description
Wilson’s disease is a genetic disorder which causes the body to accumulate too much copper. This causes liver failure and brain damage in affected patients. Wilson’s is a rare disease because it affects about 1 in 30,000 people (250k worldwide). The drugs currently used to treat Wilson’s are copper-binders, but there are two major problems with these:
1) Toxicity: these drugs have severe side effects, and treatment course often has to stop
2) Administration: tablets need to be taken before every meal for the rest of the patient’s life
