Wilson's Disease is an inherited disorder that causes copper to build up in the body. Normally, the liver filters out extra copper, but in Wilson's Disease this process doesn't work. As copper accumulates in the liver, brain, eyes, and other organs, it can cause serious damage. Early diagnosis and treatment are essential to prevent complications.
Symptoms vary depending on age and which organs are affected. Common signs include:
Wilson's Disease is caused by genetic factors that disrupt normal copper metabolism:
At GastroDoxs, we specialize in the diagnosis and management of Wilson's Disease with personalized care plans that include chelation and zinc therapy, dietary counseling, and ongoing monitoring. Our multidisciplinary team-featuring gastroenterologists, neurologists, dietitians, and transplant experts-works together to support your long-term health. Ready to take control of your copper levels and protect your liver and brain? Book an appointment with our Wilson's Disease specialist in Katy today.
We've successfully treated more than 1K patients, helping individuals improve their digestive health and overall well-being through expert, personalized care.
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Wilson's Disease is a genetic disorder in which the body can't properly remove excess copper. This leads to copper building up in the liver, brain, eyes, and other organs, causing damage if left untreated.
Diagnosis involves blood tests to measure copper and ceruloplasmin levels, a 24-hour urine copper test, an eye exam to check for Kayser-Fleischer rings, and sometimes genetic testing for ATP7B mutations.
A hepatologist or gastroenterologist typically manages Wilson's Disease, while a neurologist may help if there are movement or cognitive symptoms. Dietitians and transplant specialists can also be part of your care team.
The ICD-10 code for Wilson's Disease is E83.01, classified under disorders of copper metabolism.
A low-copper diet is recommended. Focus on fresh fruits, vegetables, lean meats, and whole grains. Avoid high-copper foods such as shellfish, nuts, chocolate, mushrooms, and organ meats.
Yes. Wilson's Disease often appears in children, teens, or young adults. Early symptoms may include fatigue, abdominal discomfort, behavioral changes, or tremors.
There is no cure, but lifelong treatment with copper-chelating medications and/or zinc therapy can effectively control copper levels and prevent organ damage.
Surgery is rare and reserved for cases of acute liver failure. In those situations, a liver transplant may be necessary to restore normal copper metabolism.
Regular follow-up every 3-6 months is important. Blood and urine tests track copper levels and liver function, and imaging or eye exams may be scheduled as needed.
Yes. GastroDoxs in Katy offers expert care for Wilson's Disease, with a multidisciplinary team that includes gastroenterologists, neurologists, dietitians, and transplant specialists.