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

angiokeratoma corporis diffusum
alpha-galactosidase a deficiency
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Morbi
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Self Emploid(private Clinic)

Morbi

Shri M P Shah Medical College Jamnagar

M B B S

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Medical Component OfHCM

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Govt. Medical College, Jammu

M.S (General Surgery )

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Chennai
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GRH Madurai

Mbbs

Madurai Medical College

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LLRM

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Dankuni, Hooghly, West Bengal
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Medvarsity, Apollo Hospital.

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Lucknow
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Vivekananda Polyclinic And Institute Of Medical Sciences

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Vivekananda Polyclinic And Institute of Medical Sciences

DNB OPHTHALMOLOGY

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Hyderabad
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Apollo Institutions of Medical Sciences

Student

AIMS&R

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Barpali
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Self Employed. Now Doing My Practice

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Sri Padmavathi Medical College for Women

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