Dear Patient,

At your examination in my office, you were diagnosed with cardiac symptoms that are frequently associated with an inherited disease called Fabry disease. This disease is progressive and may result in addition to heart disease, in kidney failure and/or stroke later in life. The other most common symptoms you may experience are episodes of pain in the hands and feet, heat and cold intolerance, an inability to perspire and a red to purple rash in the belt to knee area. There is also a variant of the disease that is limited to the heart.

If you have any of these symptoms, or you have a family history of Fabry disease, I would like to recommend that you contact the Fabry Program at Albany Medical Center at 1-800-456-9900 or at their website fabrydisease.com. At your request, you will be provided with a testing kit that you may take to your doctor’s office. Your doctor will draw a blood sample, and use the kit for testing the level of the enzyme alpha-galactosidase in your blood. This enzyme is absent or present at low levels in patients with Fabry disease, and therefore is diagnostic for Fabry disease.

Early diagnosis for Fabry disease is important now, since a treatment has become available that will stop the progression of the course of the disease and relieve the early symptoms. This treatment replaces the missing enzyme, which in turn will degrade deposits of a fatty substance in your blood vessels. These deposits are the cause of most of the symptoms of Fabry disease. Enzyme replacement therapy will help to relieve or prevent most symptoms. The treatment was FDA approved in April 2003. For more information contact Albany Medical Center.

I strongly recommend that you request your test kit and take advantage of the opportunity for early diagnosis and treatment.

Yours sincerely,