Literature DB >> 6395627

A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis.

A Ohlsson, U Sieck, W Cumming, M Akhtar, F Serenius.   

Abstract

A case of early onset Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis is reported. A literature review of Bartter's syndrome supports the hypothesis that the findings in this infant constitute a specific variant of Bartter's syndrome inherited in an autosomal recessive mode. Fetal polyuria in Bartter's syndrome leads to hydramnios, and the excess fluid causes premature birth. This variant of Bartter's syndrome should be included in the differential diagnosis of hydramnios, especially if the woman has had previous hydramnios resulting in a perinatal death. The disorder responds to treatment with indomethacin.

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Year:  1984        PMID: 6395627     DOI: 10.1111/j.1651-2227.1984.tb17793.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  14 in total

1.  Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome.

Authors:  R Vargas-Poussou; D Feldmann; M Vollmer; M Konrad; L Kelly; L P van den Heuvel; L Tebourbi; M Brandis; L Karolyi; S C Hebert; H H Lemmink; G Deschênes; F Hildebrandt; H W Seyberth; L M Guay-Woodford; N V Knoers; C Antignac
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

2.  Renal sonographic patterns in Bartter's syndrome.

Authors:  S A Al-Rasheed; P J Patel; T M Kolawole; M Al-Mugeiren; T Malabarey; A Al Salloum; A S Al-Herbish; N A Al-Jurayyan
Journal:  Pediatr Radiol       Date:  1996

3.  Pre-pubertal growth in the hyperprostaglandin E syndrome.

Authors:  C Seidel; S Reinalter; H W Seyberth; K Schärer
Journal:  Pediatr Nephrol       Date:  1995-12       Impact factor: 3.714

4.  Causes of increased renal medullary echogenicity in Turkish children.

Authors:  A Nayir; A Kadioğlu; A Sirin; S Emre; E Tonguç; I Bilge
Journal:  Pediatr Nephrol       Date:  1995-12       Impact factor: 3.714

Review 5.  Isoforms of renal Na-K-2Cl cotransporter NKCC2: expression and functional significance.

Authors:  Hayo Castrop; Jurgen Schnermann
Journal:  Am J Physiol Renal Physiol       Date:  2008-05-21

6.  Growth from birth to adulthood in a patient with the neonatal form of Bartter syndrome.

Authors:  W Proesmans; G Massa; M Vanderschueren-Lodeweyckx
Journal:  Pediatr Nephrol       Date:  1988-04       Impact factor: 3.714

Review 7.  Prostanoids in paediatric kidney diseases.

Authors:  H W Seyberth; A Leonhardt; B Tönshoff; N Gordjani
Journal:  Pediatr Nephrol       Date:  1991-09       Impact factor: 3.714

8.  "Neonatal variant" of Bartter syndrome presenting with acidosis.

Authors:  A Ammenti; S Montali
Journal:  Pediatr Nephrol       Date:  1996-02       Impact factor: 3.714

9.  Rare independent mutations in renal salt handling genes contribute to blood pressure variation.

Authors:  Weizhen Ji; Jia Nee Foo; Brian J O'Roak; Hongyu Zhao; Martin G Larson; David B Simon; Christopher Newton-Cheh; Matthew W State; Daniel Levy; Richard P Lifton
Journal:  Nat Genet       Date:  2008-04-06       Impact factor: 38.330

10.  Typical Features of Amelogenesis Imperfecta in Two Patients with Bartter's Syndrome.

Authors:  Hercílio Martelli-Júnior; Shirlene Pimentel Ferreira; Paula Cristina B Pereira; Ricardo D Coletta; Sibele Nascimento de Aquino; Débora Marques Miranda; Ana Cristina Simões E Silva
Journal:  Nephron Extra       Date:  2012-12-18
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