非典型Apert综合征:颅骨、面中部和下颌骨的顺序和节段性牵张成骨。

Nobuyuki Mitsukawa, Kaneshige Satoh, Takashi Hayashi, Tadashi Morishita, Yoshiaki Hosaka
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引用次数: 3

摘要

我们描述了一个患有Apert综合征的男孩,包括颅骨畸形和并指畸形(肢头并指畸形),尽管颅内高压,突出眼和面中发育不全是轻微的。除额眶牵张外,我们对他进行下颌牵张和Le Fort III型面中牵张治疗,效果良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atypical Apert syndrome: sequential and segmental distraction osteogenesis of the skull, midface, and mandible.

We describe a boy with Apert syndrome, including cranial deformities and syndactyly (acrocephalosyndactyly), though intracranial hypertension, exophthalmos, and midfacial hypoplasia were mild. We treated him by mandibular distraction, in addition to fronto-orbital distraction, and Le Fort III midfacial distraction, with good results.

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