Literature DB >> 1403458

Congenital sodium diarrhea with a partial defect in jejunal brush border membrane sodium transport, normal rectal transport, and resolving diarrhea.

J M Fell1, M P Miller, Y Finkel, I W Booth.   

Abstract

Defective jejunal sodium/proton exchange causes severe, congenital secretory diarrhea. We report a boy who presented typically in utero, but in whom diarrhea resolved during the first year of life. Pregnancy was complicated by polyhydramnios, and an ultrasound at 31 weeks showed a distended fetal small intestine. The abdomen was grossly distended at birth, and profuse secretory diarrhea began immediately. He subsequently thrived on breast milk and electrolyte supplements. Studies of jejunal brush border sodium/proton exchange at 6 months showed a partial defect. Nonequilibrium rectal dialysis showed rectal sodium and potassium transport to be intact. Diarrhea lessened after 9 months, and the patient subsequently required occasional laxatives. These observations suggest that there is a spectrum of congenital abnormality in this exchanger, and that in children with incomplete defects normal colonic sodium salvage can subsequently mask net small intestinal secretion.

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Year:  1992        PMID: 1403458     DOI: 10.1097/00005176-199208000-00002

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  5 in total

1.  Nucleotide sequence of the Na+/H+ exchanger-8 in patients with congenital sodium diarrhea.

Authors:  Michel Baum; Martin G Martin; Ian W Booth; Christer Holmberg; Katherine Twombley; Qiuyu Zhang; Jyothsna Gattineni; Orson Moe
Journal:  J Pediatr Gastroenterol Nutr       Date:  2011-11       Impact factor: 2.839

2.  Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea.

Authors:  Andreas R Janecke; Peter Heinz-Erian; Jianyi Yin; Britt-Sabina Petersen; Andre Franke; Silvia Lechner; Irene Fuchs; Serge Melancon; Holm H Uhlig; Simon Travis; Evelyne Marinier; Vojislav Perisic; Nina Ristic; Patrick Gerner; Ian W Booth; Satu Wedenoja; Nadja Baumgartner; Julia Vodopiutz; Marie-Christine Frechette-Duval; Jan De Lafollie; Rabindranath Persad; Neil Warner; C Ming Tse; Karan Sud; Nicholas C Zachos; Rafiquel Sarker; Xinjun Zhu; Aleixo M Muise; Klaus-Peter Zimmer; Heiko Witt; Heinz Zoller; Mark Donowitz; Thomas Müller
Journal:  Hum Mol Genet       Date:  2015-09-10       Impact factor: 6.150

3.  Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea.

Authors:  Peter Heinz-Erian; Thomas Müller; Birgit Krabichler; Melanie Schranz; Christian Becker; Franz Rüschendorf; Peter Nürnberg; Bernard Rossier; Mihailo Vujic; Ian W Booth; Christer Holmberg; Cisca Wijmenga; Giedre Grigelioniene; C M Frank Kneepkens; Stefan Rosipal; Martin Mistrik; Matthias Kappler; Laurent Michaud; Ludwig-Christoph Dóczy; Victoria Mok Siu; Marie Krantz; Heinz Zoller; Gerd Utermann; Andreas R Janecke
Journal:  Am J Hum Genet       Date:  2009-01-29       Impact factor: 11.025

4.  Congenital sodium diarrhea in a neonate presenting as acute renal failure.

Authors:  Abdulkarim S Al Makadma; Samhar I Al-Akash; Ibtisam Al Dalaan; Muath Al Turaiki; Souheil M Shabib
Journal:  Pediatr Nephrol       Date:  2004-06-04       Impact factor: 3.714

5.  Pathophysiology of Intestinal Na+/H+ exchange.

Authors:  Michael A Gurney; Daniel Laubitz; Fayez K Ghishan; Pawel R Kiela
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2017-01
  5 in total

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