Fabry disease - Wikipedia, the free encyclopedia Fabry disease (/ˈfɑːbri/) (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is a rare genetic lysosomal storage disease, inherited in an X-linked manner. Fabry disease can cause
Fabry Disease - Diseases & Conditions - Medscape Reference Fabry disease is an X-linked lysosomal disorder that leads to excessive deposition of neutral glycosphingolipids in the vascular endothelium of several organs and in epithelial and smooth muscle cells. Progressive endothelial accumulation of glycosphingol
Fabry disease - Genetics Home Reference Fabry disease is an inherited disorder that results from the buildup of a particular type of fat, called globotriaosylceramide, in the body's cells. Beginning in childhood, this buildup causes signs and symptoms that affect many parts of the body. Charact
Fabry Disease Information Page: National Institute of Neurological Disorders and Stroke (NINDS) Fabry's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). ... Prepared by: Office of Communications and Public Liaison National Institute of Neurological Disorders and Stroke National Institutes of
Fabry Disease: Read About Life Expectancy and Treatment Read about Fabry disease, a genetic condition with symptoms such as decreased sweating, fever, small, raised reddish-purple blemishes, burning sensations in the hands, and gastrointestinal difficulties. ... Kidney Failure Kidney failure can occur from an
National Fabry Disease Foundation The National Fabry Disease Foundation (NFDF) is an organization dedicated to supporting the Fabry disease community ... Dani Goes to Fabry Family Camp ... by Dawn Laney with illustrator Michael Johnson. We are very pleased to announce two new educational
OMIM Entry - # 301500 - FABRY DISEASE - OMIM - Online Mendelian Inheritance in Man 301500 - FABRY DISEASE - ANGIOKERATOMA CORPORIS DIFFUSUM;; ANDERSON-FABRY DISEASE;; HEREDITARY DYSTOPIC LIPIDOSIS;; ALPHA-GALACTOSIDASE A DEFICIENCY;; GLA DEFICIENCY;; CERAMIDE TRIHEXOSIDASE ... Contributors:
FabryPage - Fabry Support & Information Group What is Fabry Disease Fabry Disease: Fabry disease results from abnormal deposits of a particular fatty substance (called globotriaosylcera-mide) in blood vessel walls throughout the body. The primary defect which allows this to occur is the inherited def
What is fabry disease | Fabry Support Group Australia Over many years, GL-3 slowly accumulates and builds up in the walls of blood vessels body fluids and the cells of many tissues, particularly the nerves, kidney, heart and eyes. Involvement of major organ systems such as the heart, kidney, skin and brain m
Fabry Disease - The Doctor's Doctor Fabry disease is a rare X-linked recessive lysosomal storage disease. Patients typically have angiokeratomas distributed between the umbilicus and knees, painful crises of the hands and feet, and renal, ophthalmologic, and cardiac abnormalities. An 11-yea
