Solem R Christian, Martz Martin, Weiss Elie, Reese Patricia, Kawamoto Henry, Lee Justine C
Cleft Palate Craniofac J. 2017 Jan;54(1):100-108. doi: 10.1597/15-217. Epub 2016 Jan 11.
Antley-Bixler syndrome is a rare form of craniosynostosis characterized by unique clinical features that present particular challenges to long-term treatment. Typical craniofacial features include midface hypoplasia, trapezoidocephaly, frontal bossing, ocular proptosis, low-set protrusive ears, and choanal atresia. A staged surgical approach including fronto-orbital and midface advancements is required for intracranial pressure reduction, globe protection, airway patency, and malocclusion. In this case report, the combined, longitudinal surgical and orthodontic treatment strategies employed to correct severe facial deformity in a long-term 21-year survivor of Antley-Bixler syndrome are reviewed.
安特利-比克斯勒综合征是一种罕见的颅缝早闭形式,其特征是独特的临床特征,给长期治疗带来特殊挑战。典型的颅面特征包括面中部发育不全、梯形头、额部隆起、眼球突出、低位突出耳和后鼻孔闭锁。为降低颅内压、保护眼球、保持气道通畅和矫正咬合不正,需要采用包括额眶和面中部前移的分期手术方法。在本病例报告中,回顾了用于矫正一名21岁长期存活的安特利-比克斯勒综合征患者严重面部畸形的联合、纵向手术和正畸治疗策略。