Fabry disease is an inherited disorder that results from the buildup of a particular type of fat, called globotriaosylceramide, in the body's cells.
Fabry disease (/ ˈ f ɑː b r i /) (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is ...
Fabry disease is caused by the lack of or faulty enzyme needed to metabolize lipids, fat-like substances that include oils, waxes, and fatty acids.
WebMD looks at the causes, symptoms, and treatment of Fabry disease, an inherited condition that brings on a variety of symptoms, including pain in the hands and feet.
Information about the group and this disease. Join the group free of charge and receive a newsletter.
The National Fabry Disease Foundation (NFDF) is an organization dedicated to supporting the Fabry disease community
What is Fabry Disease. Fabry Disease: Fabry disease results from abnormal deposits of a particular fatty substance (called globotriaosylcera-mide) in blood vessel ...
Fabry's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
Fabry–Pérot interferometers or etalons are used in optical modems, spectroscopy, lasers, and astronomy. A related device is the Gires–Tournois etalon.
Is there any treatment for Fabry disease? What is the prognosis for Fabry disease? What research is being done on Fabry disease?