What are the symptoms of Fabrys disease?
Fabry’s disease in an inherited disease that causes a significant defect in the body’s metabolic process. The symptoms of Fabry’s disease range from minor to extremely severe.IdentificationFabry’s disease occurs when the body lacks the enzyme needed to metabolize lipids, which include fatty acids, waxes and oils. This enzyme deficiency causes abnormal deposits of fatty substances to build up on the walls of the body’s blood vessels.Symptoms – ChildrenThe symptoms of Fabry’s disease commonly begins in childhood. In addition to brief episodes of intense pain and burning sensations in the hands and feet, the child also develops a dark red, spotted skin rash. Other symptoms include nausea, vomiting, headaches, vertigo, fevers, gastrointestinal problems and hypohidrosis.Symptoms – MalesFabry’s disease progresses slowly; serious symptoms associated with the disease commonly affect males between the ages of 30 and 45. Serious symptoms include kidney disease, prolapse of the mitral valve in th
