Fabry disease
A rare X-linked inherited lysosomal storage disorder characterized by deficiency of the enzyme alpha-galactosidase A. It results in the accumulation of glycolipids in the blood vessels and tissues. Signs and symptoms include hypertension, cardiomyopathy, angiokeratomas, neuropathy, hypohidrosis, keratopathy, proteinuria, and renal failure.
Disease Alternative Name
Top Fabry disease Doctors on Curofy
Top doctors who continously share their opinions on Fabry disease
Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S
Medical Component OfHCM
Remained Incharge Medical Officer with Hon'Ble C.M of J and K for More Than 20 Years from Jan 2000 To October 2020
Govt. Medical College, Jammu
M.S (General Surgery )
GRH Madurai
Mbbs
Madurai Medical College
MBBS
LLRM
Senior Resident
Private
23 Yrs. Experienced Homoeopathic Practitioner & 10 Yrs. Experienced Clinical Dietitian
Medvarsity, Apollo Hospital.
Fellowship in Applied Nutrition.
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