How To Treat Fabry's Disease

Fabry's disease is a rare genetic disorder that affects every one in forty thousand males and some females. It is caused by a deficiency of the enzyme alpha-galactosidase A. Multiple regions of the body can be affected by Fabry's disease, and symptoms range from ringing in the ears and hearing loss to a burning sensation covering the skin, gastrointestinal problems, and major organ complications. Patients with Fabry's disease have a life expectancy of fifty-eight years in males and seventy-five in females, though the disease is far more prevalent in men than women. If you or a loved one have been diagnosed with Fabry's disease, there are some treatment options available that may reduce symptoms and improve the condition.

Hemodialysis

Over time, Fabry's disease causes fat to build up on cells and organ tissues, which can lead to kidney failure and heart complications. Patients are unable to make the natural enzyme alpha-GAL, which helps break down certain fats so the body can process and pass them. In many cases, the first course of treatment for Fabry's disease is enzyme replacement therapy.

In cases where kidney failure or damage has occurred, hemodialysis is the go-to treatment. Dialysis performs the processes kidneys no longer can by separating water, salt, and other toxins from the body. The processes undertaken during dialysis keep a patient's body functioning, but it is most frequently done while a patient is waiting for a transplant.

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