Literature DB >> 9261039

Familial focal segmental glomerulosclerosis: nine cases in four families and review of the literature.

P F Faubert1, J G Porush.   

Abstract

Idiopathic focal segmental glomerulosclerosis (FSGS) is a common cause of glomerular disease. Although previous case reports suggesting a familial form of the disease exist in the literature, its significance has not been emphasized. We report on our experience with nine cases in four families, as well as a review of the literature, and provide evidence that a familial form of FSGS might represent a distinct genotypic and phenotypic subset of idiopathic FSGS.

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Year:  1997        PMID: 9261039     DOI: 10.1016/s0272-6386(97)90062-7

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  3 in total

1.  A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.

Authors:  D H Cohn; T Shohat; M Yahav; T Ilan; G Rechavi; L King; M Shohat
Journal:  Am J Hum Genet       Date:  2000-08-04       Impact factor: 11.025

Review 2.  Integrating human and rodent data to identify the genetic factors involved in chronic kidney disease.

Authors:  Michael R Garrett; Marcus G Pezzolesi; Ron Korstanje
Journal:  J Am Soc Nephrol       Date:  2010-02-04       Impact factor: 10.121

3.  Two new families with hereditary minimal change disease.

Authors:  Hassib Chehade; Francois Cachat; Eric Girardin; Samuel Rotman; Antonio Jorge Correia; Florence Fellmann; Olivier Bonny
Journal:  BMC Nephrol       Date:  2013-03-22       Impact factor: 2.388

  3 in total

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