Literature DB >> 11876110

Neonatal Bartter syndrome.

Mamta N Muranjan1, Vishakha C Kantharia, S B Bavdekar, Ujjwala Kabde, Ramesh C Parmar.   

Abstract

A case of neonatal Bartter syndrome is reported. The baby born pre-term following a pregnancy complicated by polyhydramnios, presented at 7 months of age with failure to thrive, gastroenteritis and facial dysmorphisms. An unusual feature was the absence of the classical biochemical abnormality of hypochloremic alkalosis early in the course of the disease. Metabolic acidosis was the initial manifestation at 5 weeks of age. Awareness of this presentation is important to avoid delay in diagnosis and treatment.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11876110     DOI: 10.1007/bf02723788

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  14 in total

1.  Biochemical examination of mother's urine is useful for prenatal diagnosis of Bartter syndrome.

Authors:  Y Matsushita; Y Suzuki; N Oya; S Kajiura; K Okajima; O Uemura; K Suzumori
Journal:  Prenat Diagn       Date:  1999-07       Impact factor: 3.050

2.  Bartter syndrome in Costa Rica: a description of 20 cases.

Authors:  G Madrigal; P Saborio; F Mora; G Rincon; L M Guay-Woodford
Journal:  Pediatr Nephrol       Date:  1997-06       Impact factor: 3.714

3.  Recurrent hydramnios as a result of fetal Bartter's syndrome (a case report).

Authors:  M H Shah; O D Batwar; S V Parulekar
Journal:  J Postgrad Med       Date:  1991-04       Impact factor: 1.476

4.  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

5.  Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder.

Authors:  D Landau; H Shalev; M Ohaly; R Carmi
Journal:  Am J Med Genet       Date:  1995-12-04

6.  Neonatal Bartter syndrome--use of indomethacin in the newborn period and prevention of growth failure.

Authors:  F E Mackie; E M Hodson; L P Roy; J F Knight
Journal:  Pediatr Nephrol       Date:  1996-12       Impact factor: 3.714

7.  [Fetal polyuria and decrease of electrolytes in amniotic fluid as principal markers of neonatal Bartter's syndrome].

Authors:  A Di Pietro; M R Proverbio; V Tammaro; E Riccio; C Santoro; C Sarnelli; F Cicale
Journal:  Pediatr Med Chir       Date:  1997 Jul-Aug

8.  Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome.

Authors:  H W Seyberth; W Rascher; H Schweer; P G Kühl; O Mehls; K Schärer
Journal:  J Pediatr       Date:  1985-11       Impact factor: 4.406

9.  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

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

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

View more
  1 in total

1.  Bartter's Syndrome Masquerading as a Neurometabolic Disorder.

Authors:  H R Ramamurthy; M Kanitkar; U Raju
Journal:  Med J Armed Forces India       Date:  2011-07-21
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.