Beckwith-Wiedemann syndrome is an overgrowth syndrome complicated both
phenotypically and genetically. The aim of the study is to present a few cases of newborn …

Diastema has a multifactorial etiology. Some of the etiological factors are clear-cut, whereas
others are controversial and not completely elucidated. It is very important to define the …

1. What are the components of the craniofacial skeleton? The craniofacial skeleton is
composed of the neurocranium (cranial vault and cranial base) and the viscerocranium …

Management of the neonate with airway obstruction begins in the fetal period with initial
evaluation involving the use of ultrasound and magnetic resonance imaging. The airway can …

El síndrome de Beckwith-Wiedemann es una alteración congénita con diversas
manifestaciones clínicas, de entre las cuales las más prevalentes son la macroglosia (97%) …

Macroglosia reprezintă o problemă importantă a pediatrului, prin prisma tulburărilor de
alimentaţie şi de respiraţie pe care aceasta le implică. Limba anormal de mare poate fi …

abstract The Beckwith–Wiedemann syndrome is a congenital disorder with diverse clinical
manifestations, among which the most prevalent are, macroglossia (97%), gigantism (88%) …

TH È SE Page 1 Les glossoplasties de réduction : présentation d’une nouvelle technique TH È
SE Présentée et publiquement soutenue devant LA FACULTÉ DE MÉDECINE DE MARSEILLE …

抄録 Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by
macroglossia, omphalocele, and macrosomia. Macroglossia is the predominant finding, with …

抄録 Opitz syndrome is a congenital disorder characterized by facial anomaly (ocular
hypertelorism, widow's peak, broad nasal bridge, and strabismus), laryngotracheal and …