Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping

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 postpo...

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Autores principales: Degrugillier, Fanny, Simon, Stéphanie, Aissat, Abdel, Remus, Natascha, Mekki, Chadia, Decrouy, Xavier, Hatton, Aurélie, Hinzpeter, Alexandre, Hoffmann, Brice, Sermet‐Gaudelus, Isabelle, Callebaut, Isabelle, Fanen, Pascale, Prulière‐Escabasse, Virginie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878083/
https://www.ncbi.nlm.nih.gov/pubmed/31788264
http://dx.doi.org/10.1002/ccr3.2443
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author Degrugillier, Fanny
Simon, Stéphanie
Aissat, Abdel
Remus, Natascha
Mekki, Chadia
Decrouy, Xavier
Hatton, Aurélie
Hinzpeter, Alexandre
Hoffmann, Brice
Sermet‐Gaudelus, Isabelle
Callebaut, Isabelle
Fanen, Pascale
Prulière‐Escabasse, Virginie
author_facet Degrugillier, Fanny
Simon, Stéphanie
Aissat, Abdel
Remus, Natascha
Mekki, Chadia
Decrouy, Xavier
Hatton, Aurélie
Hinzpeter, Alexandre
Hoffmann, Brice
Sermet‐Gaudelus, Isabelle
Callebaut, Isabelle
Fanen, Pascale
Prulière‐Escabasse, Virginie
author_sort Degrugillier, Fanny
collection PubMed
description 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.
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spelling pubmed-68780832019-11-29 Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping Degrugillier, Fanny Simon, Stéphanie Aissat, Abdel Remus, Natascha Mekki, Chadia Decrouy, Xavier Hatton, Aurélie Hinzpeter, Alexandre Hoffmann, Brice Sermet‐Gaudelus, Isabelle Callebaut, Isabelle Fanen, Pascale Prulière‐Escabasse, Virginie Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2019-09-27 /pmc/articles/PMC6878083/ /pubmed/31788264 http://dx.doi.org/10.1002/ccr3.2443 Text en © 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Degrugillier, Fanny
Simon, Stéphanie
Aissat, Abdel
Remus, Natascha
Mekki, Chadia
Decrouy, Xavier
Hatton, Aurélie
Hinzpeter, Alexandre
Hoffmann, Brice
Sermet‐Gaudelus, Isabelle
Callebaut, Isabelle
Fanen, Pascale
Prulière‐Escabasse, Virginie
Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
title Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
title_full Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
title_fullStr Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
title_full_unstemmed Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
title_short Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
title_sort unsolved severe chronic rhinosinusitis elucidated by extensive cftr genotyping
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878083/
https://www.ncbi.nlm.nih.gov/pubmed/31788264
http://dx.doi.org/10.1002/ccr3.2443
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