Literature DB >> 1915522

Chronic metabolic alkalosis in an infant with cystic fibrosis.

P Eigenmann1, G Délèze, H Kuchler.   

Abstract

A 6-month-old infant suffering from cystic fibrosis is reported. In spite of an apparently appropriate treatment and in absence of respiratory infection, the patient showed progressive anorexia, intermittent vomiting and weight loss. These non-specific signs and symptoms could all be explained by metabolic alkalosis and disappeared immediately after oral supplementation with sodium and potassium chloride. This unusual metabolic complication should be searched for in every cystic fibrosis infant with unexplained anorexia and failure to thrive.

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Year:  1991        PMID: 1915522     DOI: 10.1007/bf02072631

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  7 in total

1.  Heat prostration in fibrocystic disease of the pancreas and other conditions.

Authors:  W R KESSLER; D H ANDERSEN
Journal:  Pediatrics       Date:  1951-11       Impact factor: 7.124

2.  Metabolic alkalosis and salt depletion in cystic fibrosis.

Authors:  S N Arvanitakis; C C Lobeck
Journal:  J Pediatr       Date:  1973-03       Impact factor: 4.406

3.  Metabolic alkalosis in cystic fibrosis.

Authors:  R P Gottlieb
Journal:  J Pediatr       Date:  1971-12       Impact factor: 4.406

4.  Early diagnosis of cystic fibrosis by means of sweat microosmometry.

Authors:  M H Schöni; R Kraemer; P Bähler; E Rossi
Journal:  J Pediatr       Date:  1984-05       Impact factor: 4.406

5.  Changing feeding trends as a cause of electrolyte depletion in infants with cystic fibrosis.

Authors:  J J Laughlin; M S Brady; H Eigen
Journal:  Pediatrics       Date:  1981-08       Impact factor: 7.124

6.  Hypoelectrolytemia and metabolic alkalosis in infants with cystic fibrosis.

Authors:  R C Beckerman; L M Taussig
Journal:  Pediatrics       Date:  1979-04       Impact factor: 7.124

7.  Developmental outcome in children exposed to chloride-deficient formula.

Authors:  A Willoughby; H A Moss; V S Hubbard; B B Bercu; B I Graubard; P M Vietze; C C Chang; H W Berendes
Journal:  Pediatrics       Date:  1987-06       Impact factor: 7.124

  7 in total
  1 in total

Review 1.  Electrolyte abnormalities in cystic fibrosis: systematic review of the literature.

Authors:  Elisabetta Scurati-Manzoni; Emilio F Fossali; Carlo Agostoni; Enrica Riva; Giacomo D Simonetti; Maura Zanolari-Calderari; Mario G Bianchetti; Sebastiano A G Lava
Journal:  Pediatr Nephrol       Date:  2013-12-11       Impact factor: 3.714

  1 in total

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