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Ocular, Ear and Renal Manifestations of Alport Syndrome in Three Iranian Families
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نویسنده
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Davari Mohammad Hossein ,Gheytasi Hoda ,Golboei S. Mohammad Hossein ,Rezvani Mohammad Reza
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منبع
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zahedan journal of research in medical sciences - 2014 - دوره : 16 - شماره : 11 - صفحه:59 -59
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چکیده
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Alport syndrome is a genetic disorder of basement membranes caused by mutations in type iv collagen network. it was first identified by dr. alport in 1927. its major clinical manifestations are included: glomerulopathy, sensory hearing loss, anterior lenticonus, and the prevalence of alports’ gene in general population is about 1 in 5000 and the disease prevalence is 1 in 10000 [1-3]. here we report ocular, ear and renal manifestations of alport syndrome in 3 families that living in the east city of iran, birjand, and we have followed all of this family for 6 years so far.
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کلیدواژه
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Alport ,Manifestations ,Ocular
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آدرس
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birjand university of medical sciences, Department of Ophthalmology, Aterosclerosis Research Center, Birjand University of Medical Sciences, Birjand, Iran, ایران, University of Barcelona, Barcelona, Spain, PhD Student of Genetic, Translational Research Laboratory, University of Barcelona, Barcelona, Spain, اسپانیا, birjand university of medical sciences, Department of ENT, Birjand University of Medical Sciences, Birjand, Iran, ایران, birjand university of medical sciences, Department of Internal Medicine, Birjand University of Medical Sciences, Birjand, Iran, ایران
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Authors
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