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's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
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.
What is Fabry Disease. Fabry Disease: Fabry disease results from abnormal deposits of a particular fatty substance (called globotriaosylcera-mide) in blood vessel ...
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.
The National Fabry Disease Foundation (NFDF) is an organization dedicated to supporting the Fabry disease community
Information about the group and this disease. Join the group free of charge and receive a newsletter.
Fabry disease is an inherited disorder that results from the buildup of a particular type of fat, called globotriaosylceramide, in the body's cells.
Important It is possible that the main title of the report Fabry Disease is not the name you expected. Please check the synonyms listing to find the alternate name(s ...
Fabry disease is uncommon, although research suggests that Fabry mutations may be more frequent than previously thought in cryptogenic stroke patients.