Background Progress in medical branches that has taken place since the first child with
Goldenhare syndrome (GS) had been described in 1952 by Maurice Goldenhar, facilitated …

The temporomandibular joint (TMJ) consists of the mandibular condyle and the articular
eminence of the temporal bone. The morphological development of the TMJ during prenatal …

OBJECTIVES: Goldenhar syndrome (GS) is a relatively common developmental disorder
characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and …

Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial
development. Major features include midface hypoplasia, micrognathia, microtia, conductive …

Congenital deformities of the temporomandibular joint (TMJ) complex present as a
heterogeneous continuum of growth disturbances of the mandibular condyle, articular …

Goldenhar syndrome is a rare congenital defect characterized by ocular symptoms including
(epibulbar dermoids, microphthalmia, anophthalmia, eyes asymmetry/dysmorphy, cleft …

Abstract Background Goldenhar Syndrome is a rare congenital condition, typically
characterized by craniofacial abnormalities and vertebral malformations. Due to its rare and …

Objetivo: Presentar nuestra experiencia en el diagnóstico y el tratamiento de 42 pacientes
con síndrome de Goldenhar. Método: Se realizó un estudio descriptivo, observacional y …

Aim: The aim of this cross-sectional study was to evaluate, via cone-beam computed
tomography, the long-term postoperative outcome in children treated with mandibular …

Goldenhar syndrome is a multifactorial congenital anomaly that involves structures that
develop from the first and second pharyngeal arches. In this report, we present a clinical …