Literature DB >> 9630034

Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms.

S Reinalter1, H Devlieger, W Proesmans.   

Abstract

This baby boy was born after a pregnancy complicated by severe polyhydramnios at a gestational age of 28 weeks. Analysis of the amniotic fluid had shown a high chloride content, but normal concentrations of sodium, potassium, and calcium. After birth he displayed extreme polyuria, severe renal sodium and chloride loss, and marked hypercalciuria. Five weeks after birth, his sodium chloride loss turned into renal potassium loss, along with a marked decrease in urine output. All these features are characteristic of the neonatal variant of Bartter syndrome. He was discharged after 11 weeks with oral supplements of sodium chloride, potassium gluconate, and 500 ml of fluid. The follow-up for a period of 6 years showed a surprising evolution: he has no hypokalemic alkalosis, no polyuria, and no hypercalciuria; growth and development are within the normal ranges and, at the time of writing, he is a healthy boy needing no medication and with no medical problems whatsoever.

Entities:  

Mesh:

Year:  1998        PMID: 9630034     DOI: 10.1007/s004670050433

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  8 in total

Review 1.  Pathophysiology and clinical presentations of salt-losing tubulopathies.

Authors:  Hannsjörg W Seyberth
Journal:  Pediatr Nephrol       Date:  2015-07-16       Impact factor: 3.714

2.  Neonatal Bartter syndrome.

Authors:  Mamta N Muranjan; Vishakha C Kantharia; S B Bavdekar; Ujjwala Kabde; Ramesh C Parmar
Journal:  Indian J Pediatr       Date:  2002-01       Impact factor: 1.967

Review 3.  A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.

Authors:  Anna K Lee; Patrick Ryan Potts
Journal:  J Mol Biol       Date:  2017-03-11       Impact factor: 5.469

Review 4.  Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects.

Authors:  Hannsjörg W Seyberth; Karl P Schlingmann
Journal:  Pediatr Nephrol       Date:  2011-04-19       Impact factor: 3.714

5.  Antenatal bartter syndrome: a review.

Authors:  Y Ramesh Bhat; G Vinayaka; K Sreelakshmi
Journal:  Int J Pediatr       Date:  2012-02-28

6.  Transient Antenatal Bartter's Syndrome: A Case Report.

Authors:  Michelle Meyer; Margarita Berrios; Christina Lo
Journal:  Front Pediatr       Date:  2018-03-12       Impact factor: 3.418

7.  A Case Report and Literature Review of a Novel Mutation in the MAGED2 Gene of a Patient With Severe Transient Polyhydramnios.

Authors:  Xiaoxia Wu; Le Huang; Caiqun Luo; Yang Liu; Jianmin Niu
Journal:  Front Pediatr       Date:  2021-12-01       Impact factor: 3.418

8.  A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter's syndrome with 4 years follow-up.

Authors:  Mingsheng Ma; Mengqi Zhang; Yu Zhou; Fengxia Yao; Min Wei; Zhenghong Li; Zhengqing Qiu
Journal:  BMC Nephrol       Date:  2021-12-11       Impact factor: 2.388

  8 in total

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