Retrusão do terço médio da face é característica das disostoses sindrômicas. Falta de projeção e deficiência estrutural podem ser responsáveis pelo fenômeno, mas estes nunca foram avaliados adequadamente tridimensionalmente. O objetivo deste estudo é analisar a interface entre a base do crânio e a face, o volume dos ossos do terço médio da face e o volume e estrutura dos componentes da órbita, para fornecer uma compreensão da etiopatogenia da deficiência do terço médio da face e da dismorfologia ocular. Crianças com tomografia computadorizada, na ausência de qualquer intervenção cirúrgica, foram incluídas. As informações demográficas foram obtidas para três grupos (Apert, Crouzon, Controle). As tomografias computadorizadas foram digitalizad...
Background:. In Crouzon’s syndrome, cranial base deformities begin sequentially in the anterior cran...
Apert syndrome, or acrocephalosyndactyly type I, is a craniofacial dysostosis, an autosomal dominant...
The aim of this study was to describe directional and fluctuating mandibular asymmetry over time in ...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
A Síndrome de Apert é caracterizada por craniossinosteses e sindactilia dos dedos das mãos e dos pés...
textabstractObjective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve t...
A major concern in FGFR2 craniofaciosynostosis is oculo-orbital disproportion, such that orbital mal...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
Apert syndrome, or acrocephalosyndactyly type I, is a craniofacial dysostosis, an autosomal dominant...
Abstract Background A 9-year-old male showed severe defects in midface structures, which resulted in...
The aim of this study was to compare changes in dental arch morphology between patients with Crouzon...
Apert syndrome is a rare acrocephalosyndactyly syndrome characterised by craniosynostosis, midface h...
Background:. In Crouzon’s syndrome, cranial base deformities begin sequentially in the anterior cran...
Apert syndrome, or acrocephalosyndactyly type I, is a craniofacial dysostosis, an autosomal dominant...
The aim of this study was to describe directional and fluctuating mandibular asymmetry over time in ...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
A Síndrome de Apert é caracterizada por craniossinosteses e sindactilia dos dedos das mãos e dos pés...
textabstractObjective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve t...
A major concern in FGFR2 craniofaciosynostosis is oculo-orbital disproportion, such that orbital mal...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
Apert syndrome, or acrocephalosyndactyly type I, is a craniofacial dysostosis, an autosomal dominant...
Abstract Background A 9-year-old male showed severe defects in midface structures, which resulted in...
The aim of this study was to compare changes in dental arch morphology between patients with Crouzon...
Apert syndrome is a rare acrocephalosyndactyly syndrome characterised by craniosynostosis, midface h...
Background:. In Crouzon’s syndrome, cranial base deformities begin sequentially in the anterior cran...
Apert syndrome, or acrocephalosyndactyly type I, is a craniofacial dysostosis, an autosomal dominant...
The aim of this study was to describe directional and fluctuating mandibular asymmetry over time in ...