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Coexistant of Fabry Disease and IgA Glomerulonephritis in a 39 Year Old Male
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نویسنده
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Makhlough Atieh ,Emadi Tarkami Fatemeh
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منبع
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iranian journal of pathology - 2009 - دوره : 4 - شماره : 2 - صفحه:92 -95
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چکیده
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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 withproteinuria 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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کلیدواژه
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Fabry disease ,IgA Glomerulonephritis ,Iran
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آدرس
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Sary University of medical sciences, Dept of Internal Medicine, ایران, Sary University of medical sciences, Dept of Internal Medicine, ایران
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پست الکترونیکی
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makhlough@yahoo.com
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Authors
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