书目名称 | Handbook of Cystic Fibrosis |
编辑 | Amy G. Filbrun,Thomas Lahiri,Clement L Ren |
视频video | http://file.papertrans.cn/422/421123/421123.mp4 |
概述 | Concise yet complete overview of the epidemiology, pathophysiology, and clinical features of cystic fibrosis and an in-depth review of the most up-to-date methods of diagnosis, symptom management, and |
图书封面 |  |
描述 | 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. |
出版日期 | Book 2016 |
关键词 | CFTR mutations; Cystic Fibrosis; Cystic Fibrosis manifestations; Pulmonary; Respiratory medicine |
版次 | 1 |
doi | https://doi.org/10.1007/978-3-319-32504-0 |
isbn_softcover | 978-3-319-32502-6 |
isbn_ebook | 978-3-319-32504-0 |
copyright | Springer International Publishing Switzerland 2016 |