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Wilson's disease to is one of the rare kinds of inherited disorders that affects the liver brain and various other organs. Symptoms of this disease include feeling of constant fatigue and lack of appetite. There are also extreme feelings of muscle and abdominal pain and fluid buildup, which is then followed with muscle stiffness and uncontrolled movements.
HOW IS WILSON'S DISEASE DIAGNOSED?
Diagnosis of Wilson's Disease is challenging because symptoms are difficult to distinguish from other diseases. Gastroenterologists may order for blood and urine tests for monitoring liver function. Eye examination, biopsy of liver tissue and genetic testing are diagnostic methods to confirm Wilson's Disease
HOW IS WILSON'S DISEASE TREATED?
A health care provider will treat Wilson disease with a lifelong effort to reduce and control the amount of copper in the body. Treatment may include
• changes in eating, diet, and nutrition
• a liver transplant
DID YOU KNOW?
The problem can turn out to be fatal in case the same is not treated on time with complete liver failure.