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

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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Bibliographic Details
Main Author: D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand (Author)
Format: Book
Published: Tehran University of Medical Sciences, 1993-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a  D.D. Farhud; T.Rezaie Jami; M.R. Khosh-sorour; M. Islami; B.Broumand  |e author 
245 0 0 |a "Preliminary Report: EVIDENCE OF AUTOSOMAL RECESSIVE FORM OF ALPORT SYNDROME IN IRAN " 
260 |b Tehran University of Medical Sciences,   |c 1993-06-01T00:00:00Z. 
500 |a 2251-6085 
500 |a 2251-6093 
520 |a 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. 
546 |a EN 
690 |a Alport syndrorme 
690 |a Hereditary nephritis 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Iranian Journal of Public Health, Vol 22, Iss 1-4 (1993) 
787 0 |n https://ijph.tums.ac.ir/index.php/ijph/article/view/1595 
787 0 |n https://doaj.org/toc/2251-6085 
787 0 |n https://doaj.org/toc/2251-6093 
856 4 1 |u https://doaj.org/article/2b366107dbeb4da996115032cc07c955  |z Connect to this object online.