Cystic Fibrosis is an inheritable disease/ genetic disorder that affects mostly the lungs but also the pancreas, liver, kidneys and intestine.Lung infections are hard to treat in general because mucous is thick and sluggish and result in increased scarring (fibrosis) of the lungs. Symptoms include salty-tasting skin, frequent lung infections including pneumonia or bronchitis, Wheezing or shortness of breath etc.
Related Journals of Cystic Fibrosis
Journal of Cystic Fibrosis, Inflammation in cystic fibrosis lung disease, Journal of Medicine, Thorax, Hereditary Genetics Current Research, Molecular and Genetic Medicine Journal, Fibrogenesis & Tissue Repair
All Published work is licensed under a Creative Commons Attribution 4.0 International License
Copyright © 2017 All rights reserved. iMedPub Last revised : April 30, 2017