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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?
While it is best suited to visit a General Physician when you have a Fabry Disease, this disease usually starts in childhood and is more common in men than women. Fabry Disease is a condition wherein a certain type of fatty substance builds up in the body and it essentially narrows the blood vessels, which in turn, can hurt the kidneys, skin, heart, brain and nervous system. While it can take a long time to get diagnosed with the Fabry Disease, the doctor normally conducts a physical exam to check its occurrence.
HOW IS FABRY DISEASE TREATED?
Pain management through analgesics, anticonvulsants along with a variety of nonsteroidal anti-inflammatory drugs is done. However, at times, special procedures like ERT may be the only solution for treating the same. Other clinical treatments are available in advanced countries like Europe but the prices go extremely high.
DID YOU KNOW?
Fabry disease is estimated to affect 1 in 40,000 males. Fabry disease is a progressive disorder and symptoms that affect the kidneys, heart, or brain most often occur when patients are age 30 to 45 years.