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

Yalcin E., Kiper N., DOĞRU ERSÖZ D., Ozcelik U., ASLAN A. T.

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

  • 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).