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

Authors

  • Atieh Makhlough Dept. of Internal Medicine, Sary University of medical sciences, Sary, Iran
  • Seyyedeh Fatemeh Emadi tarkami Dept. of Internal Medicine, Sary University of medical sciences, Sary, Iran
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 were in favor  of  Fabry disease in associate with IgA nephropathy. Fabry's disease associated with IgA nephropathy apparently is extremely rare, and the present case is among few reported cases in literature.  

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Journal title

volume 4  issue 2

pages  92- 95

publication date 2009-04-01

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