Also known as storage disorder, Fabry Disease leads to the production of a fatty substance in the body that eventually affects various parts of the body such as skin, brain, kidney, heart and nervous system as well. Patients suffering from this genetic disorder lack alpha-galactosidase in their body, an enzyme that breaks the fatty acids. This particular disease can lead to heart attacks, kidney failure, osteoporosis, high blood pressure, etc. In such cases patients experience pain in their hands and feet. The other visible symptoms include hearing problems, poor vision, red spots between belly button and knee, stomach ache and abnormal sweating.
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 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.