Clinical features and treatment approaches in cystic fibrosis with pseudo-Bartter syndrome

Yalcin, E; Kiper, N; Dogru, DENİZ; Ozcelik, KADRİYE; Aslan, AT

doi:10.1179/146532805x45719

Clinical features and treatment approaches in cystic fibrosis with pseudo-Bartter syndrome

Atıf İçin Kopyala

Yalcin E., Kiper N., Dogru D., Ozcelik U., Aslan A.

ANNALS OF TROPICAL PAEDIATRICS, cilt.25, sa.2, ss.119-124, 2005 (SCI-Expanded)

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
Hacettepe Üniversitesi Adresli: Evet

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).