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G Ital Nefrol ; 41(3)2024 06 28.
Artigo em Italiano | MEDLINE | ID: mdl-38943326

RESUMO

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.


Assuntos
Síndrome de Bartter , Fibrose Cística , Humanos , Fibrose Cística/complicações , Fibrose Cística/genética , Fibrose Cística/diagnóstico , Síndrome de Bartter/complicações , Síndrome de Bartter/diagnóstico , Síndrome de Bartter/genética , Masculino , Feminino , Hiponatremia/etiologia , Alcalose/etiologia , Pré-Escolar , Criança
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