Dental and maxillofacial features of noonan ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Dental and maxillofacial features of noonan syndrome: case series of ten patients
Auteur(s) :
Lutz, Jean-Christophe [Auteur]
Université de Strasbourg [UNISTRA]
Nanomédecine Régénérative [NanoRegMed]
Nicot, Romain [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Médicaments et biomatériaux à libération contrôlée: mécanismes et optimisation - Advanced Drug Delivery Systems - U 1008 [MBLC - ADDS]
Schlund, Matthias [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Schaefer, Elise [Auteur]
Centre Hospitalier Universitaire [Strasbourg] [CHU Strasbourg]
Laboratoire de Génétique Médicale [LGM]
Bornert, Fabien [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Fioretti, Florence [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Ferri, Joel [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Médicaments et biomatériaux à libération contrôlée: mécanismes et optimisation - Advanced Drug Delivery Systems - U 1008 [MBLC - ADDS]
Université de Strasbourg [UNISTRA]
Nanomédecine Régénérative [NanoRegMed]
Nicot, Romain [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Médicaments et biomatériaux à libération contrôlée: mécanismes et optimisation - Advanced Drug Delivery Systems - U 1008 [MBLC - ADDS]
Schlund, Matthias [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Schaefer, Elise [Auteur]
Centre Hospitalier Universitaire [Strasbourg] [CHU Strasbourg]
Laboratoire de Génétique Médicale [LGM]
Bornert, Fabien [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Fioretti, Florence [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Ferri, Joel [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Médicaments et biomatériaux à libération contrôlée: mécanismes et optimisation - Advanced Drug Delivery Systems - U 1008 [MBLC - ADDS]
Titre de la revue :
Journal of cranio-maxillo-facial surgery . official publication of the European Association for Cranio-Maxillo-Facial Surgery
Nom court de la revue :
J Craniomaxillofac Surg
Numéro :
48
Pagination :
242-250
Date de publication :
2020-02-06
ISSN :
1878-4119
Mot(s)-clé(s) en anglais :
Noonan syndrome
Giant cells
Dentofacial deformities
Orthodontics
Orthognathic surgery
Maxillofacial abnormalities
Giant cells
Dentofacial deformities
Orthodontics
Orthognathic surgery
Maxillofacial abnormalities
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Noonan syndrome (NS) is a relatively common congenital multiple-anomaly syndrome, resembling Turner syndrome, but without chromosomal anomaly. Besides the unusual facies, the maxillofacial and dental features of patients ...
Lire la suite >Noonan syndrome (NS) is a relatively common congenital multiple-anomaly syndrome, resembling Turner syndrome, but without chromosomal anomaly. Besides the unusual facies, the maxillofacial and dental features of patients with NS are not well-summarized in the literature. The aim of this study was to describe these features and propose specific treatment guidelines for practitioners involved in oral and maxillofacial care. A retrospective multicentric study was conducted of 14 patients who were referred for NS screening. In total, 10 patients were found to carry a mutation involved in NS or NS-related disorders. Fifty percent of the mutations affected PTPN11. All patients presented with the typical extraoral features, such as macrocephaly, hypertelorism, ptosis, triangular face shape and ear dystrophy. Intraoral manifestations, including malocclusion (maxillary transversal deficiency, crossbite, anterior open-bite and class II malocclusion), dental anomalies (delayed eruption, agenesis and dystrophy, odontoma) and radiologic jaw lesions were identified in five out of 10 patients. These findings were searched in a review of the literature to obtain a comprehensive description of oral and maxillofacial features in patients with NS. The proposed treatment guidelines emphasize frequent coagulation anomalies that need to be considered prior to surgery. Early dental assessment and yearly follow-up with oral prophylaxis are recommended. Orthodontics and orthognathic surgery are also of primary importance in the management of NS patients.Lire moins >
Lire la suite >Noonan syndrome (NS) is a relatively common congenital multiple-anomaly syndrome, resembling Turner syndrome, but without chromosomal anomaly. Besides the unusual facies, the maxillofacial and dental features of patients with NS are not well-summarized in the literature. The aim of this study was to describe these features and propose specific treatment guidelines for practitioners involved in oral and maxillofacial care. A retrospective multicentric study was conducted of 14 patients who were referred for NS screening. In total, 10 patients were found to carry a mutation involved in NS or NS-related disorders. Fifty percent of the mutations affected PTPN11. All patients presented with the typical extraoral features, such as macrocephaly, hypertelorism, ptosis, triangular face shape and ear dystrophy. Intraoral manifestations, including malocclusion (maxillary transversal deficiency, crossbite, anterior open-bite and class II malocclusion), dental anomalies (delayed eruption, agenesis and dystrophy, odontoma) and radiologic jaw lesions were identified in five out of 10 patients. These findings were searched in a review of the literature to obtain a comprehensive description of oral and maxillofacial features in patients with NS. The proposed treatment guidelines emphasize frequent coagulation anomalies that need to be considered prior to surgery. Early dental assessment and yearly follow-up with oral prophylaxis are recommended. Orthodontics and orthognathic surgery are also of primary importance in the management of NS patients.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
Inserm
Université de Lille
Inserm
Université de Lille
Collections :
Date de dépôt :
2021-01-20T15:59:20Z
2024-02-19T10:00:59Z
2024-02-19T10:00:59Z