Subject: Clinical medicine
Year: 2012
Type: Article
Type: NonPeerReviewed
Title: Cisticna fibroza- klinicka prezentacija, dijagnoza i tretman
Author: Dimitrovska Ivanova, Marija
Author: Karakolevska Ilova, Marija
Author: Dimitrovska, Ljupka
Abstract: Cystic fibrosis (CF) or mucoviscidosis is the most common inherited disease of white race. Is a heterogeneous multisystem disease that affects many epithelial organs, especially exocrine glands. Clinically important phenomena in the lining of the bronchus and lung, pancreas, bile ducts, intestine, salivary, sweat glands and seminal ducts. But most of the patients have chronic lung disease, pancreatic insufficiency, and increased concentration of chloride in the sweat that forms the famous triad of cystic fibrosis. Prognosis of most patients with cystic fibrosis determines chronic pulmonary disease and it is still a major cause of death in these patients.
Publisher:
Relation: https://eprints.ugd.edu.mk/1947/
Identifier: oai:eprints.ugd.edu.mk:1947
Identifier: https://eprints.ugd.edu.mk/1947/1/Cisticna%20fibroza%20za%20Medicus%201.pdfIdentifier: Dimitrovska Ivanova, Marija and Karakolevska Ilova, Marija and Dimitrovska, Ljupka (2012) Cisticna fibroza- klinicka prezentacija, dijagnoza i tretman. Medicus. ISSN 1857-5994
