AN INTRODUCTION TO FABRY DISEASE

   Fabry disease is an inherited, progressive disease that occurs worldwide among all ethnic groups.

   Fabry disease may lead to a shortened life span due to decreased kidney and heart functions. It occurs in about 1 in 40,000 males. Although symptoms occur in childhood and adolescence, the disease is usually first diagnosed in men in their early forties.

   If you exhibit the common symptoms, or if there is a history of Fabry disease in your family, you may be at increased risk of kidney failure, heart attack or stroke. While there is no cure at present, there is an effective treatment available. This treatment, following early diagnosis, will replace the missing enzyme and prevent or stop the development of any permanent damage to the kidney and cardiovascular system.

THERE IS A TREATMENT

FDA approved Enzyme replacement therapy April 2003

   An effctive enzyme replacement therapy for Fabry disease is available. A blood test is all that is neccessary to find out if an individual has Fabry disease.

   We offer testing to individuals who exhibit symptoms (confirmed by a physician) or have a family history of Fabry disease. This testing is available across the United States and can be facilitated world- wide. Testing can be done at any age. All that is required for the test is a blood sample. Fill out and submit the questionnaire to determine your eligibility for testing.

For additional information, please call
1-800-456-9900 at the Albany Medical Center.