Literature DB >> 17555949

[Renal tubular dysgenesis and mutation in the renin gene].

J Bacchetta1, F Dijoud, R Bouvier, G Putet, M-C Gubler, P Cochat.   

Abstract

Renal tubular dysgenesis is a severe and rare disorder of the renal development characterized by fetal anuria, oligohydramnios and early death from pulmonary hypoplasia and refractory arterial hypotension. We report on a female patient who presented with anuria in the neonatal period, requiring peritoneal dialysis until 5 months of age with unexpected diuresis recovery at 2 months of age. Clinical, histological and pathophysiological issues are discussed for this disease related to a mutation in the renin gene.

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Year:  2007        PMID: 17555949     DOI: 10.1016/j.arcped.2007.04.012

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  6 in total

1.  Autosomal Recessive Renal Tubular Dysgenesis Caused by a Founder Mutation of Angiotensinogen.

Authors:  Min-Hua Tseng; Shih-Ming Huang; Jing-Long Huang; Wen-Lang Fan; Martin Konrad; Steven W Shaw; Reyin Lien; Hui-Ping Chien; Jhao-Jhuang Ding; Tai-Wei Wu; Jeng-Daw Tsai; Ya-Chung Tian; Hwei-Jen Lee; Po-Jen Cheng; Jen-Fu Hsu; Shih-Hua Lin
Journal:  Kidney Int Rep       Date:  2020-08-20

2.  A further case of renal tubular dysgenesis surviving the neonatal period.

Authors:  Mitsugu Uematsu; Osamu Sakamoto; Toshihiro Ohura; Nobuhiko Shimizu; Kenichi Satomura; Shigeru Tsuchiya
Journal:  Eur J Pediatr       Date:  2008-05-14       Impact factor: 3.183

Review 3.  Renal tubular dysgenesis.

Authors:  Marie-Claire Gubler
Journal:  Pediatr Nephrol       Date:  2013-05-01       Impact factor: 3.714

4.  AGTR1-related Renal Tubular Dysgeneses May Not Be Fatal.

Authors:  Ebru Burcu Demirgan; Seha Saygili; Nur Canpolat; Lale Sever; Isin Kilicaslan; Doruk Taylan; Salim Caliskan; Fatih Ozaltin
Journal:  Kidney Int Rep       Date:  2020-12-13

Review 5.  Expanding the clinical spectrum of autosomal-recessive renal tubular dysgenesis: Two siblings with neonatal survival and review of the literature.

Authors:  Krista M Vincent; Afrah Alrajhi; Joanna Lazier; Brigitte Bonin; Sarah Lawrence; Gabrielle Weiler; Christine M Armour
Journal:  Mol Genet Genomic Med       Date:  2022-03-14       Impact factor: 2.473

6.  Functional tests to guide management in an adult with loss of function of type-1 angiotensin II receptor.

Authors:  Daan H H M Viering; Anneke P Bech; Jeroen H F de Baaij; Eric J Steenbergen; A H Jan Danser; Jack F M Wetzels; René J M Bindels; Jaap Deinum
Journal:  Pediatr Nephrol       Date:  2021-03-25       Impact factor: 3.714

  6 in total

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