"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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Tehran University of Medical Sciences,
1993-06-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_2b366107dbeb4da996115032cc07c955 | ||
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. |