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Doctors for Fabry Disease in Guduvanchery, Kanchipuram
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Fabry Disease is defined as a rare genetic lysosomal storage disease. Research shows that this disease is kind of inherited in the X-linked manner or form. One of the common symptoms of the same includes a dysfunctional metabolism rate that can cause extreme obesity and weight loss cycles. The early symptoms start off in childhood and are often misdiagnosed.
HOW IS FABRY DISEASE DIAGNOSED?
The exact diagnosis may take a longer time. The general physician may ask for a blood test or a DNA test followed by physical examination.
HOW IS FABRY DISEASE TREATED?
Enzyme replacement therapy is prescribed. Various medications for pain relief, stomach ailments and blood pressure is also recommended.
DID YOU KNOW?
Fabry disease leads to reduced life expectancy in patients.