Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital Malformations.

Détails

ID Serval
serval:BIB_5F7B52BFFD3F
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital Malformations.
Périodique
Pediatrics and Neonatology
Auteur(s)
Broome M., Vial Y., Jacquemont S., Sergi C., Kamnasaran D., Giannoni E.
ISSN
2212-1692 (Electronic)
ISSN-L
1875-9572
Statut éditorial
Publié
Date de publication
2016
Volume
57
Numéro
1
Pages
65-68
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Syngnathia is an extremely rare condition involving congenital fusion of the maxilla with the mandible. Clinical presentations vary from simple mucosal bands (synechiae) to complete bony fusion (synostosis). Most cases are unilateral incomplete fusions. We report the case of a severely growth-retarded newborn infant with complete synostosis of the mandible with the maxilla and the zygoma associated with cleft palate, choanal atresia, deafness, delayed cerebral white matter development, and genital and limb malformations. Extensive genetic analysis did not reveal any mutations. This association of multiple congenital malformations may represent an entity distinct from previously described syndromes associated with syngnathia.
Mots-clé
Abnormalities, Multiple/surgery, Cleft Palate/surgery, Humans, Infant, Newborn, Male, Mandible/abnormalities, Maxilla/abnormalities, Synostosis/surgery, Zygoma/abnormalities
Pubmed
Web of science
Open Access
Oui
Création de la notice
31/01/2014 14:42
Dernière modification de la notice
20/08/2019 14:17
Données d'usage