Cystic fibrosis (CF) is the most prevalent inheritable chronic disease in Caucasian children. The clinical syndrome of kwashiorkor is a well-recognized complication of CIF The edema of the face can be seen in kwashiorkor. As doll-like face is very rare and underestimated clinical presentation of CF patients complicated with hypoproteinemia we evaluated demographic features and laboratory characteristics of 5 patients diagnosed as CF with doll-like face. Methods: Between June 2005 and January 2008, 115 children were diagnosed as having CIF enrolled in our center Five infants that were diagnosed as CF with doll-like face before the age of 6 months participitated in study. Results: The incidence of doll-like face younger than 6 months of age w...
Severe anemia is reported to occur rarely in patients with cystic fibrosis (CF). This study aimed to...
AbstractPresentation of cystic fibrosis with a rash is rare, with only 19 previously reported cases....
Cystic fibrosis is the most common life shortening autosomal recessive disorder in Caucasians. The m...
Cystic fibrosis or mucoviscidosis is the most common genetic disease in the Caucasian race character...
Introduction: Cystic fibrosis (CF) is an autosomal recessive genetic disorder, more prevalent in the...
Cystic fibrosis (CF) is an autosomal recessive affliction triggered by genetic mutations in the cyst...
The diagnosis of cystic fibrosis (CF) can be confusing when only a part of the typical symptoms is p...
BACKGROUND: Many children with cystic fibrosis grow poorly and are malnourished. This study was unde...
The authors report on three infants with cystic fibrosis (CF), with different genotypes, presenting ...
Background: Pseudo-Bartter’s syndrome (PBS) is a clinical entity characterized by hypokalemia, hypo-...
BackgroundUniversal newborn screening changed the way medical providers think about the presentation...
Cystic fibrosis (CF) is an autosomal recessive disease commonly found among the Caucasian population...
Hair depigmentation is very rare presentation of cystic fibrosis (CF). We present 3.5-month-old fema...
Introduction: Pseudo-Bartter syndrome (PBS) is a rare manifestation of Cystic fibrosis (CF) and can ...
Diagnosing cystic fibrosis: blood, sweat, and tears Making a diagnosis of cystic fibrosis has lifelo...
Severe anemia is reported to occur rarely in patients with cystic fibrosis (CF). This study aimed to...
AbstractPresentation of cystic fibrosis with a rash is rare, with only 19 previously reported cases....
Cystic fibrosis is the most common life shortening autosomal recessive disorder in Caucasians. The m...
Cystic fibrosis or mucoviscidosis is the most common genetic disease in the Caucasian race character...
Introduction: Cystic fibrosis (CF) is an autosomal recessive genetic disorder, more prevalent in the...
Cystic fibrosis (CF) is an autosomal recessive affliction triggered by genetic mutations in the cyst...
The diagnosis of cystic fibrosis (CF) can be confusing when only a part of the typical symptoms is p...
BACKGROUND: Many children with cystic fibrosis grow poorly and are malnourished. This study was unde...
The authors report on three infants with cystic fibrosis (CF), with different genotypes, presenting ...
Background: Pseudo-Bartter’s syndrome (PBS) is a clinical entity characterized by hypokalemia, hypo-...
BackgroundUniversal newborn screening changed the way medical providers think about the presentation...
Cystic fibrosis (CF) is an autosomal recessive disease commonly found among the Caucasian population...
Hair depigmentation is very rare presentation of cystic fibrosis (CF). We present 3.5-month-old fema...
Introduction: Pseudo-Bartter syndrome (PBS) is a rare manifestation of Cystic fibrosis (CF) and can ...
Diagnosing cystic fibrosis: blood, sweat, and tears Making a diagnosis of cystic fibrosis has lifelo...
Severe anemia is reported to occur rarely in patients with cystic fibrosis (CF). This study aimed to...
AbstractPresentation of cystic fibrosis with a rash is rare, with only 19 previously reported cases....
Cystic fibrosis is the most common life shortening autosomal recessive disorder in Caucasians. The m...