HCPs - Discover How Your Practice Can Be The First For Fabry Patients.
Fabry Affects the Whole Body — The effects of Fabry disease are variable and may occur in many parts of the body. Every person...
HCPs: Explore a treatment option for some adults with a confirmed Fabry disease diagnosis.
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 ...
Jun 6, 2019 · Fabry disease is a rare inherited disorder of glycosphingolipid (fat) metabolism resulting from the absent or markedly deficient activity of the ...
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, 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 ...
Fabry disease is an inherited disorder that can be potentially life-threatening. Once one person has been diagnosed with Fabry disease, it is likely that other ...
Fabry disease is a progressive, destructive and potentially life-threatening disease. Fabry disease can affect males and females of all ethnic and cultural ...
May 23, 2023 · Fabry disease is caused by deficiency of the lysosomal enzyme alpha-galactosidase A involved in the metabolism of globotriaosylceramide (GL-3).