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.
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