أعرض في EDS

Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping

التفاصيل البيبلوغرافية
العنوان: Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
المؤلفون: Aurélie Hatton, Isabelle Callebaut, Xavier Decrouy, Stéphanie Simon, Chadia Mekki, Natascha Remus, Abdel Aissat, Fanny Degrugillier, Brice Hoffmann, Alexandre Hinzpeter, Isabelle Sermet-Gaudelus, Pascale Fanen, Virginie Prulière-Escabasse
المصدر: Clinical Case Reports
Clinical Case Reports, Vol 7, Iss 11, Pp 2128-2134 (2019)
بيانات النشر: John Wiley and Sons Inc., 2019.
سنة النشر: 2019
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Chronic rhinosinusitis, lcsh:Medicine, Pulmonary infection, Case Report, macromolecular substances, Case Reports, 030204 cardiovascular system & hematology, Cystic fibrosis, cystic fibrosis, 03 medical and health sciences, 0302 clinical medicine, Rare mutations, Medicine, Functional studies, CFTR, Genotyping, lcsh:R5-920, business.industry, chronic rhinosinusitis, lcsh:R, General Medicine, respiratory system, medicine.disease, 030220 oncology & carcinogenesis, Immunology, functional studies, lcsh:Medicine (General), business
الوصف: Severe chronic rhinosinusitis in children should alert clinicians and extensive CFTR genotyping should be performed. We propose that thorough clinical and functional assessment in severe chronic rhinosinusitis is valuable to discover rare mutations which could be treated by CFTR correctors to postpone pulmonary infection.
اللغة: English
تدمد: 2050-0904
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93d4433a8202d90eb53d8c930323c04b
http://europepmc.org/articles/PMC6878083
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....93d4433a8202d90eb53d8c930323c04b
قاعدة البيانات: OpenAIRE
الوصف
تدمد:20500904