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Coexistant of Fabry Disease and IgA Glomerulonephritis in a 39 year old male

Atieh Makhlough; Seyyedeh Fatemeh Emadi tarkami

Volume 4, Issue 2 , April 2009, , Pages 92-95

Abstract
    Anderson-Fabry disease is a rare inherited X-linked lysosomal storage disease caused by deficiency of the enzyme alpha-galactosidase A. Hereby we report a 39 year old male that presented with proteinuria and edema. Histopathologic, immunofluorescence and ultrastractural examination of renal tissue ...  Read More