%0 Journal Article %T Coexistant of Fabry Disease and IgA Glomerulonephritis in a 39 year old male %J Iranian Journal of Pathology %I Farname Inc in collaboration with Iranian Society of Pathology %Z 1735-5303 %A Makhlough, Atieh %A Emadi tarkami, Seyyedeh Fatemeh %D 2009 %\ 04/01/2009 %V 4 %N 2 %P 92-95 %! Coexistant of Fabry Disease and IgA Glomerulonephritis in a 39 year old male %K Fabry disease %K IgA Glomerulonephritis %K Iran %R %X   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.   %U https://ijp.iranpath.org/article_8979_4befab940c0f6cca81c48da33767d8a8.pdf