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?
Enzyme replacement therapy is one of the treatment methods for Fabry Disease. This is however a very costly treatment method
DID YOU KNOW?
It affects the patient right from the childhood and is more common in males.