Fabry disease is a very rare lipids storage disease caused by a deficiency in the enzyme Alpha Galactosidase A. in childhood the symptoms are usually fatigue, pain in the arms and legs and lack of perspiration. Later on, other symptoms such as strokes, protein in the urine, renal failure and cardiac hypertrophy can appear.
The clinic treats most Fabry patients in Israel. Correct treatment usually prevents the advancement of the disease. The clinic also provides diagnostic services, including genetic tests using gene sequencing.
When should you suspect Fabry? If there's an unexplained stroke at a young age, unexplained protein in the urine, cardiac hypertrophy, neuropathic pains and multiple red spots on the skin (called angiokeratomas).

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