Clinical features and treatment approaches in cystic fibrosis with pseudo-Bartter syndrome
ANNALS OF TROPICAL PAEDIATRICS, cilt.25, sa.2, ss.119-124, 2005 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 25 Sayı: 2
- Basım Tarihi: 2005
- Doi Numarası: 10.1179/146532805x45719
- Dergi Adı: ANNALS OF TROPICAL PAEDIATRICS
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.119-124
- Gazi Üniversitesi Adresli: Hayır
Özet
Introduction: Infants with cystic fibrosis (CF) are prone to develop episodes of hyponatraemic, hypochloraemic dehydration with metabolic alkalosis, which are biochemical hallmarks of the pseudo-Bartter syndrome (PB).