Coexistant of Fabry Disease and IgA Glomerulonephritis in a 39 Year Old Male
عنوان مقاله: Coexistant of Fabry Disease and IgA Glomerulonephritis in a 39 Year Old Male
شناسه ملی مقاله: JR_IJP-4-2_008
منتشر شده در شماره 2 دوره 4 فصل بهار در سال 1388
شناسه ملی مقاله: JR_IJP-4-2_008
منتشر شده در شماره 2 دوره 4 فصل بهار در سال 1388
مشخصات نویسندگان مقاله:
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
خلاصه مقاله:
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
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 ofrenal 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
کلمات کلیدی: Fabry disease, IgA Glomerulonephritis, Iran
صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/302653/