Book Details
Format
Paperback / Softback
ISBN-10
3319325027
ISBN-13
9783319325026
Edition
1st ed. 2016
Publisher
Springer International Publishing AG
Imprint
Adis
Country of Manufacture
CH
Country of Publication
GB
Publication Date
Oct 20th, 2016
Print length
99 Pages
Weight
150 grams
Dimensions
20.30 x 13.50 x 0.60 cms
Product Classification:
Hereditary diseases & disordersGastroenterologyRespiratory medicine
Ksh 8,100.00
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This concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease.
This concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease. The latest guidelines are reviewed and current and emerging treatments are discussed in the latter chapters. Cystic fibrosis is an inherited condition where a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) causes loss of function. The dysfunction of CFTR results in the production of thick mucus in the lungs and digestive tract, causing pulmonary and gastrointestinal manifestations. The incidence of cystic fibrosis in Europe and the US ranges between 1 in 2,000 and 1 in 25,000.
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