دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: [Two Cases of Pseudo-Bartter Syndrome in Childhood: When to Suspect a Rare Onset Pattern of Cystic Fibrosis].
المؤلفون: Vergine, Gianluca, Fressola, Giulia, Ambroni, Maura, Gessaroli, Monica, Bigucci, Barbara, Mazzocco, Martina, Conte, Maria Luisa
المصدر: G Ital Nefrol ; ISSN:1724-5990 ; Volume:41 ; Issue:3
بيانات النشر: SIN Società Italiana di Nefrologia
سنة النشر: 2024
المجموعة: PubMed Central (PMC)
مصطلحات موضوعية: cystic fibrosis, hyponatremia, metabolic alkalosis, pediatrics, pseudo-Bartter syndrome
الوصف: 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.
نوع الوثيقة: article in journal/newspaper
اللغة: Italian
العلاقة: https://pubmed.ncbi.nlm.nih.gov/38943326Test
الإتاحة: https://pubmed.ncbi.nlm.nih.gov/38943326Test
حقوق: Copyright by Società Italiana di Nefrologia SIN, Rome,Italy.
رقم الانضمام: edsbas.E5580588
قاعدة البيانات: BASE