Cisticna fibroza- klinicka prezentacija, dijagnoza i tretman

Dimitrovska Ivanova, Marija and Karakolevska Ilova, Marija and Dimitrovska, Ljupka (2012) Cisticna fibroza- klinicka prezentacija, dijagnoza i tretman. Medicus. ISSN 1857-5994

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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.

Item Type:	Article
Subjects:	Medical and Health Sciences > Clinical medicine
Divisions:	Faculty of Medical Science
Depositing User:	Marija Dimitrovska
Date Deposited:	24 Nov 2012 16:30
Last Modified:	24 Nov 2012 16:30
URI:	https://eprints.ugd.edu.mk/id/eprint/1947

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