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. 1990 Jul;65(7):786–787. doi: 10.1136/adc.65.7.786

Pseudo-Bartter's syndrome in cystic fibrosis.

J D Kennedy 1, R Dinwiddie 1, C Daman-Willems 1, M J Dillon 1, D J Matthew 1
PMCID: PMC1792454  PMID: 2386386

Abstract

Seven cases of cystic fibrosis complicated by chronic salt depletion and failure to thrive were studied. After replacement of the salt deficit, the metabolic abnormalities resolved, and weight gain was rapid. This should be considered as a differential diagnosis in children who have been diagnosed as having cystic fibrosis, but who fail to thrive despite standard treatment.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arvanitakis S. N., Lobeck C. C. Metabolic alkalosis and salt depletion in cystic fibrosis. J Pediatr. 1973 Mar;82(3):535–536. doi: 10.1016/s0022-3476(73)80139-8. [DOI] [PubMed] [Google Scholar]
  2. Devlin J., Beckett N. S., David T. J. Elevated sweat potassium, hyperaldosteronism and pseudo-Bartter's syndrome: a spectrum of disorders associated with cystic fibrosis. J R Soc Med. 1989;82 (Suppl 16):38–43. [PMC free article] [PubMed] [Google Scholar]
  3. Dillon M. J., Shah V., Mitchell M. D. Bartter's syndrome: 10 cases in childhood. Results of long-term indomethacin therapy. Q J Med. 1979 Jul;48(191):429–446. [PubMed] [Google Scholar]
  4. SIBINGA M. S., BARBERO G. J. Studies in the physiology of sweating in cystic fibrosis. II. Elevated night sweating rates. Arch Dis Child. 1961 Oct;36:537–539. doi: 10.1136/adc.36.189.537. [DOI] [PMC free article] [PubMed] [Google Scholar]

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