Fabry disease is caused by changes in a gene. The faulty gene passed on by the mother.
Males with the faulty gene will have the disease. Females who have a single copy of the gene are called carriers. Most will not have any symptoms, but they can pass the gene to their children. Some women may be as affected as men.
Symptoms may start when you are a child or young adult. Common ones are:
- Pain and burning feeling in the hands and feet—often worse with exercise, lack of energy, or fever
- Spotted, dark reddish-purple skin wounds between the belly button and the knees
- Sweating more or less
- Problems seeing
- Delayed growth
- Ringing in the ears
- A feeling of spinning when you are not moving
As adults, men may have:
- Kidney problems
- Heart problems
- Frequent stools, diarrhea
- Problems breathing
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There is no cure for Fabry disease.
You may be given medicine to:
- Replace enzymes
- Treat pain
- Thin your blood
- Manage heart problems
The kidneys may be harmed from blood flow problems. They may need:
- Angiotensin-converting enzyme (ACE) inhibitors and/or an angiotensin receptor blockers (ARBs)—to stabilize kidney function
- Hemodialysis—if they aren't working properly
- Kidney transplantation—if kidney failure has happened
This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.
Edits to original content made by Denver Health.
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a (Alpha-Galactosidase A Deficiency; Anderson-Fabry Disease; Angiokeratoma Corporis Diffusum; Angiokeratoma Diffuse; Ceramide Trihexosidase Deficiency; GLA Deficiency; Glycolipid Lipidosis; Hereditary Dystopic Lipidosis)
Fabry Support and Information Group http://www.fabry.org
National Institute of Neurological Disorders and Stroke http://www.ninds.nih.gov
Canadian Fabry Association http://www.fabrycanada.com
Health Canada https://www.canada.ca
Fabry disease. EBSCO DynaMed Plus website. Available at: http://www.dynamed.com/topics/dmp~AN~T114633/Fabry-disease . Updated March 9, 2017. Accessed July 2, 2018.
Martins AM, D’Almeida V, Kyosen SO, et al. Guidelines to diagnosis and monitoring of Fabry disease and review of treatment experiences. J Pediatrics. 2009;155(4 Suppl):S19-S31.
NINDS Fabry disease information page. National Institute of Neurological Disorders and Stroke website. Available at: https://www.ninds.nih.gov/disorders/all-disorders/fabry-disease-information-page. Accessed July 2, 2018.
7/13/2014 DynaMed Plus Systematic Literature Surveillance http://www.dynamed.com/topics/dmp~AN~T114633/Fabry-disease . Laney DA, Bennett RL, Clarke V, et al. Fabry disease practice guidelines: recommendations of the National Society of Genetic Counselors. J Genet Couns. 2013;22(5):555-564.