Genetic diagnosis in practice: from cystic ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Genetic diagnosis in practice: from cystic fibrosis to cftr-related disorders
Auteur(s) :
Pagin, Adrien [Auteur]
IMPact de l'Environnement Chimique sur la Santé humaine (IMPECS) - ULR 4483
Sermet-Gaudelus, I. [Auteur]
Hôpital Necker - Enfants Malades [AP-HP]
Burgel, P.-R. [Auteur]
Hôpital Cochin [AP-HP]

IMPact de l'Environnement Chimique sur la Santé humaine (IMPECS) - ULR 4483
Sermet-Gaudelus, I. [Auteur]
Hôpital Necker - Enfants Malades [AP-HP]
Burgel, P.-R. [Auteur]
Hôpital Cochin [AP-HP]
Titre de la revue :
Archives de Pédiatrie
Nom court de la revue :
Arch Pediatr
Numéro :
27
Pagination :
eS25-eS29
Éditeur :
Elsevier
Date de publication :
2020-02-01
Statut de l’article :
Publié
ISSN :
0929-693X
Mot(s)-clé(s) :
Cystic fibrosis transmembrane conductance regulator (CFTR)
(CRMS)/CF screen positive inconclusive diagnosis (CFSPID)
CFTR-related metabolic syndrome
CFTR-related disorders (CFTR-RD)
Cystic fibrosis (CF)
(CRMS)/CF screen positive inconclusive diagnosis (CFSPID)
CFTR-related metabolic syndrome
CFTR-related disorders (CFTR-RD)
Cystic fibrosis (CF)
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Cystic fibrosis (CF) is a channelopathy caused by mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein. Diagnosis of CF has long relied on a combination of clinical (including gastrointestinal ...
Lire la suite >Cystic fibrosis (CF) is a channelopathy caused by mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein. Diagnosis of CF has long relied on a combination of clinical (including gastrointestinal and/or respiratory) symptoms and elevated sweat chloride concentration. After cloning of the CFTR gene in 1989, genetic analysis progressively became an important aspect of diagnosis. Although combination of sweat test and genetic analysis have simplified the diagnosis of CF in most cases, difficult situations remain, especially in cases that do not fulfill all diagnostic criteria. Such situations are most frequently encountered in patients presenting with a single-organ disease (e.g., congenital absence of the vas deferens, pancreatitis, bronchiectasis) leading to a diagnosis of CFTR-related disorder, or when the presence/ absence of CF is not resolved after newborn screening. This article reviews the diagnostic criteria of CF, with special emphasis on genetic testing. 2020 French Society of Pediatrics. Published by Elsevier Masson SAS. All rights reserved.Lire moins >
Lire la suite >Cystic fibrosis (CF) is a channelopathy caused by mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein. Diagnosis of CF has long relied on a combination of clinical (including gastrointestinal and/or respiratory) symptoms and elevated sweat chloride concentration. After cloning of the CFTR gene in 1989, genetic analysis progressively became an important aspect of diagnosis. Although combination of sweat test and genetic analysis have simplified the diagnosis of CF in most cases, difficult situations remain, especially in cases that do not fulfill all diagnostic criteria. Such situations are most frequently encountered in patients presenting with a single-organ disease (e.g., congenital absence of the vas deferens, pancreatitis, bronchiectasis) leading to a diagnosis of CFTR-related disorder, or when the presence/ absence of CF is not resolved after newborn screening. This article reviews the diagnostic criteria of CF, with special emphasis on genetic testing. 2020 French Society of Pediatrics. Published by Elsevier Masson SAS. All rights reserved.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
Institut Pasteur de Lille
Université de Lille
Institut Pasteur de Lille
Université de Lille
Date de dépôt :
2022-02-02T10:24:45Z
2022-10-05T08:12:38Z
2022-10-05T08:12:38Z
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- Pagin et al.pdf
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