Introduction: Pseudo-Bartter syndrome (PBS) is a rare manifestation of Cystic fibrosis (CF) and can often be the initial presentation in these patients, however, due to significantly overlapping symptoms it is often misdiagnosed as simple dehydration or Bartter syndrome. The objective of our study was to highlight the key features of PBS and electrolyte imbalance in CF patients helping in early and prompt diagnosis.Method: We performed a retrospective study from January 2015 to December 2019 at the Aga Khan University Hospital (AKUH), Pakistan. CF patients aged from 1-18 years, admitted at AKUH were enrolled and their laboratory data and individual charts were reviewed. Patients were categorized into three groups based on their serum electr...
Objectives: To present a case of acute hyponatriemic dehydration as a primary manifestation of cysti...
Introduction: Cystic fibrosis (CF) is an autosomal recessive genetic disorder, more prevalent in the...
The authors report on three infants with cystic fibrosis (CF), with different genotypes, presenting ...
Introduction: Pseudo-Bartter syndrome (PBS) is a rare manifestation of Cystic fibrosis (CF) and can ...
Background: Pseudo-Bartter’s syndrome (PBS) is a clinical entity characterized by hypokalemia, hypo-...
The purpose of this review article is to summarize the salt depletion and metabolic alkalosis (known...
BACKGROUND: Cystic fibrosis per se can sometimes lead to hyponatremia, hypokalemia, hypochloremia o...
Most episodes of vomiting, reduced intake and diarrhoea in children can be evaluated and treated wit...
Introduction. Infants with cystic fibrosis may fail to thrive despite recommended caloric intake be...
Background: Cystic fibrosis per se can sometimes lead to hyponatremia, hypokalemia, hypochloremia or...
Introduction. Due to increased losses of chloride and sodium in the sweat, children with cystic fibr...
Dehydration with multiple salt abnormalities is frequently encountered in the paediatric emergency d...
Çalışmada 24 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının giri...
Psödo-Bartter sendromu (PBS), hipokalemik, hipokloremik metabolik alkaloz ile karakterize klinik bir...
The diagnosis of cystic fibrosis (CF) can be confusing when only a part of the typical symptoms is p...
Objectives: To present a case of acute hyponatriemic dehydration as a primary manifestation of cysti...
Introduction: Cystic fibrosis (CF) is an autosomal recessive genetic disorder, more prevalent in the...
The authors report on three infants with cystic fibrosis (CF), with different genotypes, presenting ...
Introduction: Pseudo-Bartter syndrome (PBS) is a rare manifestation of Cystic fibrosis (CF) and can ...
Background: Pseudo-Bartter’s syndrome (PBS) is a clinical entity characterized by hypokalemia, hypo-...
The purpose of this review article is to summarize the salt depletion and metabolic alkalosis (known...
BACKGROUND: Cystic fibrosis per se can sometimes lead to hyponatremia, hypokalemia, hypochloremia o...
Most episodes of vomiting, reduced intake and diarrhoea in children can be evaluated and treated wit...
Introduction. Infants with cystic fibrosis may fail to thrive despite recommended caloric intake be...
Background: Cystic fibrosis per se can sometimes lead to hyponatremia, hypokalemia, hypochloremia or...
Introduction. Due to increased losses of chloride and sodium in the sweat, children with cystic fibr...
Dehydration with multiple salt abnormalities is frequently encountered in the paediatric emergency d...
Çalışmada 24 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının giri...
Psödo-Bartter sendromu (PBS), hipokalemik, hipokloremik metabolik alkaloz ile karakterize klinik bir...
The diagnosis of cystic fibrosis (CF) can be confusing when only a part of the typical symptoms is p...
Objectives: To present a case of acute hyponatriemic dehydration as a primary manifestation of cysti...
Introduction: Cystic fibrosis (CF) is an autosomal recessive genetic disorder, more prevalent in the...
The authors report on three infants with cystic fibrosis (CF), with different genotypes, presenting ...