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Fabry Disease

About- Fabry disease (FD) is a rare, inherited disease characterized by damaged gene with a deficiency of an enzyme called alpha-galactosidase A, that leads to a shortage of an essential enzyme results in a buildup of specific proteins in the body’s cells, causing damage to several organs including heart, lungs, kidneys, skin, brain, stomach.
 
Symptoms-
Fabry disease (FD) Abnormal corneas
Fabry disease (FD) Angina
Fabry disease (FD) Back pain in the kidney area
Fabry disease (FD) Burning sensations
Fabry disease (FD) Chest pain
Fabry disease (FD) Cloudy vision
Fabry disease (FD) Dark red spots on the skin
Fabry disease (FD) Decreased ability to sweat
Fabry disease (FD) Dizziness
Fabry disease (FD) Headache
Fabry disease (FD) Hearing loss
Fabry disease (FD) Heart enlargement
Fabry disease (FD) Heart failure
Fabry disease (FD) Heat intolerance
Fabry disease (FD) Irregular heartbeat
Fabry disease (FD) Joint pain
Fabry disease (FD) Kidney failure (in severe case)
Fabry disease (FD) Mitral valve prolapse
Fabry disease (FD) Nausea
Fabry disease (FD) Pain in the hands and feet
Fabry disease (FD) Ringing in the ears
Fabry disease (FD) Skin rash
Fabry disease (FD) Stomach problems
Fabry disease (FD) Stroke
Fabry disease (FD) Tiredness

Causes-
It is an inherited disease.
 
Specialist to visit
Endocrinologist  Endocrinologist 
Endocrinologist  Medical Genetics

Fabry disease (FD) Ask a question or view previous questions and answers on Fabry disease (FD)
References-
https://en.wikipedia.org
https://www.healthline.com
https://www.medicinenet.com
https://ghr.nlm.nih.gov
https://www.fabrydisease.org
https://www.webmd.com
https://www.medicalnewstoday.com

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