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Faecal calprotectin concentrations in young children with cystic fibrosis

Helmut Ellemunter1, Katharina Schüller2, Gratiana Steinkamp3

  • 1Cystic Fibrosis (CF) Centre at the Medical University of Innsbruck, Anichstraße 35, 6020 Innsbruck, Austria.

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|November 7, 2017
PubMed
Abstract

No abstract available in PubMed .

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Cystic Fibrosis: Pathogenesis01:23

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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
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