Fabry disease is a rare X-linked lysosomal disorder that results in excessive deposition of lipids in the tissues. Young patients usually present with stroke, skin lesions, heart attack, or renal failure. Once the diagnosis is made, an interprofessional approach is vital.
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Fabry disease is a rare genetic lysosomal storage disorder, where you don't have enough of a certain enzyme that breaks down fats.
Jul 29, 2022 · Fabry disease is an inherited disorder that results from the buildup of a type of fat, called globotriaosylceramide, in the body's cells.
Fabry disease (also known as alpha-galactosidase-A deficiency) is an inherited neurological disorder that occurs when the enzyme alpha-galactosidase-A ...
Fabry disease
Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, brain, and skin. Fabry disease is one of a group of conditions known as lysosomal storage... Wikipedia
Oct 6, 2022 · Fabry disease runs in families. It can have lots of different symptoms, including pain in the hands and feet and a specific kind of rash.
Fabry disease is a progressive, destructive and potentially life-threatening disease. Fabry disease can affect males and females of all ethnic and cultural ...