[Two Cases of Pseudo-Bartter Syndrome in Childhood: When to Suspect a Rare Onset Pattern of Cystic Fibrosis]

G Ital Nefrol. 2024 Jun 28;41(3):2024-vol3. doi: 10.69097/41-03-2024-05.
[Article in Italian]

Abstract

Cystic fibrosis is a multisystem disease with extremely variable onset, symptoms and course. One of the onset modality but also a complication of the disease is the pseudo-Bartter syndrome, characterized by hyponatremia, hypochloremic dehydration and metabolic alkalosis in absence of any renal disease. This syndrome occurs more frequently in the first year of life and has a peak in the summer. In this article, we describe two cases of cystic fibrosis associated with pseudo-Bartter syndrome in childhood. Excluding every possible cause of metabolic alkalosis associated with hyponatremia was crucial for our diagnostic pathway, and the experience gained with the first case helped a lot with the second one.

Keywords: cystic fibrosis; hyponatremia; metabolic alkalosis; pediatrics; pseudo-Bartter syndrome.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Alkalosis / etiology
  • Bartter Syndrome* / complications
  • Bartter Syndrome* / diagnosis
  • Bartter Syndrome* / genetics
  • Child
  • Child, Preschool
  • Cystic Fibrosis* / complications
  • Cystic Fibrosis* / diagnosis
  • Cystic Fibrosis* / genetics
  • Female
  • Humans
  • Hyponatremia / etiology
  • Male