Record Details

Kistifibrose

Curationis

 
 
Field Value
 
Title Kistifibrose
 
Creator Pera, D.E.
 
Subject — —
Description Cystic fibrosis is a recessively inherited inborn error of metabolism which causes abnormal functioning of mucus and sweat glands. The disease manifests itself with varying degrees of chronic lung disease, pancreatic enzyme deficiency as well as loss of salt and water in the sweat, all of which may lead to secondary complications. Treatment is aimed mainly at the removal of mucus from bronchial passages and the dietary correction of the pancreatic enzyme deficiency. As this is a chronic disease the education and support of the patient and his family are important aspects of nursing care.
 
Publisher AOSIS
 
Contributor
Date 1981-09-27
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — —
Format application/pdf
Identifier 10.4102/curationis.v4i1.510
 
Source Curationis; Vol 4, No 1 (1981); 22-27 2223-6279 0379-8577
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://curationis.org.za/index.php/curationis/article/view/510/484
 
Coverage — — —
Rights Copyright (c) 1981 D.E. Pera https://creativecommons.org/licenses/by/4.0
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