What are the treatments for fabry disease?

Fabry disease Tx. Enzyme replacement therapy and close followup with a regular doctor are the treatment for fabry disease.
Plus-minus. Fabry's, a genetic disease, is often brutal when it produces pain (especially burning palms) and interferes with the function of several organ systems. Agalsidase (replagal, fabryzyme), the replacement enzyme, is now available though hugely expensive; it reportedly helps with pain though analgesics / pain management also help. Good luck.

Related Questions

What are the advantages and disadvantages of different treatments for fabry disease?

Depends... ...On the manifestations. Pain? Kidney involvement? Heart symptoms? Rashes? Eye problems? What is going on? Treatment depends on what organs are affected. Read more...
Few available. Treatment for this inherited disease of alpha-galactosidase deficiency is an enzyme infusion available from two sources at a very expensive cost. This is not a cure but will attentuate the symptoms and allow a mostly normal lifestyle. Read more...

What is fabry disease treatment?

Fabry Disease Treatm. Treatment of fary disease is enzyme replacement therapy, but unfortunately it costs about 200000.00 us dollars per year and is not a cure but slows the progression of the disease and improves metabolism, and relieves some pain symptoms, but some patients need pain management, analgesics, anticonvulsants and non steroidal anti inflammatory drugs. Read more...

Fabry disease. Any new treatments or cure?

Treatments so far... Other than symptom management, the only real treatments available for fabry disease are enzyme replacement with agalsidase Alpha (replagal) and Agalsidase Beta (fabrazyme). These require regular infusions, and do not always lead to improvement, but do reliably halt disease progression. Read more...

Does any one know about fabry disease treatment?

Fabry Disease Treatm. Treatment of fary disease is enzyme replacement therapy, but unfortunately it costs about 200000.00 us dollars per year and is not a cure but slows the progression of the disease and improves metabolism, and relieves some pain symptoms, but some patients need pain management, analgesics, anticonvulsants and non steroidal anti inflammatory drugs. Read more...

Is there a cure fabry disease?

Not yet. Hang in there, recent research suggests some amazing breakthroughs are on the way. Google the disease and contact the major research centers. Read more...

What is "anderson-fabry" disease?

Same as Fabry. Still an inborn error of metabolism http://www.Ninds.Nih.Gov/disorders/fabrys/fabrys.Htm. Read more...

What are the tests for fabry disease?

Blood test. If the disease is suspected then the genetic tests can be done to look for the x linked galactosidase a enzyme deficiency. Read more...

What are the symptoms of fabry disease?

Fabry disease. This is a rare form of sphingolipidosis (dysfunctional metabolism of sphingolipids) due to deficiency of Alpha galactosidase enzyme a , leading to accumulation of the lipid in different organs. It presents as pain, kidney failure, hypertension, cardiomyopathy, neuropathy, fatigue, skin & eye lesions. Life expectancy is 40-60 years. Read more...
Fabry disease. This is a rare form of sphingolipidosis (dysfunctional metabolism of sphingolipids) due to deficiency of Alpha galactosidase enzyme a , leading to accumulation of the lipid in different organs. It presents as pain, kidney failure, hypertension, cardiomyopathy, neuropathy, fatigue, skin & eye lesions. Life expectancy is 40-60 years. Read more...

What sort of disorder is fabry disease?

Fabry disease. Symptoms usually begin during childhood or adolescence and include burning sensations in the hands that gets worse with exercise and hot weather and small, non-cancerous, raised reddish-purple blemishes on the skin. Lipid storage may lead to impaired arterial circulation and increased risk of heart attack or stroke. More at: http://www.Ninds.Nih.Gov/disorders/fabrys/fabrys.Htm. Read more...