"Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "

"Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "

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Alport syndrome is a progressive hereditary nephritis leading to renal failure. Nearly all of the documents declare that Alport syndrome is inherited as X-linked dominant trait and reports of autosomal inheritance form is very rare. This paper presents an Iranian large Alport family with autosomal r...

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Main Author: D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand
Format: Article
Language:English
Published: Tehran University of Medical Sciences 1993-08-01
Series:Iranian Journal of Public Health
Subjects:
Alport syndrorme
Hereditary nephritis
Online Access:http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/1501.pdf&manuscript_id=1501
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spelling doaj-44cc0d202372485bac77dd4f23ef19582020-12-02T02:57:45ZengTehran University of Medical SciencesIranian Journal of Public Health2251-60851993-08-01221-45156"Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.BroumandAlport syndrome is a progressive hereditary nephritis leading to renal failure. Nearly all of the documents declare that Alport syndrome is inherited as X-linked dominant trait and reports of autosomal inheritance form is very rare. This paper presents an Iranian large Alport family with autosomal recessive inheritance. In our patients Alport disease was confirmed with electron microscopic studies of renal biopsies.http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/1501.pdf&manuscript_id=1501Alport syndrormeHereditary nephritis
collection DOAJ
language English
format Article
sources DOAJ
author D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand
spellingShingle D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand
"Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "
Iranian Journal of Public Health
Alport syndrorme
Hereditary nephritis
author_facet D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand
author_sort D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand
title "Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "
title_short "Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "
title_full "Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "
title_fullStr "Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "
title_full_unstemmed "Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN "
title_sort "preliminary report: evidence of autosomal recessive form of alport syndrome in iran "
publisher Tehran University of Medical Sciences
series Iranian Journal of Public Health
issn 2251-6085
publishDate 1993-08-01
description Alport syndrome is a progressive hereditary nephritis leading to renal failure. Nearly all of the documents declare that Alport syndrome is inherited as X-linked dominant trait and reports of autosomal inheritance form is very rare. This paper presents an Iranian large Alport family with autosomal recessive inheritance. In our patients Alport disease was confirmed with electron microscopic studies of renal biopsies.
topic Alport syndrorme
Hereditary nephritis
url http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/1501.pdf&manuscript_id=1501
work_keys_str_mv AT ddfarhudtrezaiejamimrkhoshsorourmislamibbroumand preliminaryreportevidenceofautosomalrecessiveformofalportsyndromeiniran
_version_ 1724409808901111808

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