کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
7664184 1495132 2007 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Les manifestations respiratoires de la mucoviscidose
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Les manifestations respiratoires de la mucoviscidose
چکیده انگلیسی
Cystic fibrosis airways disease Cystic fibrosis is the most common lethal genetic disease affecting caucasians, due to a lesion of the CF gene encoding the CF transmembrane conductance regulator (CFTR). Lung disease is the primary cause of morbidity and mortality in CF. A permanent colonization of the airways with Haemophilus influenzae, Staphylococcus aureus and later Pseudomonas aeruginosa leads to progressive cycles of inflammation and infection cumulating in respiratory failure. Patients with CF are also predisposed to numerous bronchopulmorary complications as fungal infections and allergic bronchopulmorary aspergillosis, pneumothorax and hemoptysis. A standardized survey in a CF center and an early treatment of symptoms and complications delay respiratory deterioration.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Revue Francophone des Laboratoires - Volume 2007, Issue 397, December 2007, Pages 37-42
نویسندگان
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