Handbook of Cystic Fibrosis (Paperback, 1st ed. 2016)

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.

General

Imprint:	Adis International
Country of origin:	Switzerland
Release date:	October 2016
First published:	2016
Authors:	Amy G. Filbrun • Thomas Lahiri • Clement L Ren
Dimensions:	203 x 127 x 6mm (L x W x T)
Format:	Paperback
Pages:	99
Edition:	1st ed. 2016
ISBN-13:	978-3-319-32502-6
Categories:	Books > Medicine > Clinical & internal medicine > Gastroenterology Books > Medicine > Clinical & internal medicine > Respiratory medicine Books > Medicine > Clinical & internal medicine > Diseases & disorders > Congenital diseases & disorders > Hereditary diseases & disorders Promotions
LSN:	3-319-32502-7
Barcode:	9783319325026

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