Management of Apert Syndrome
堀内, 信也 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
佐藤, 博子 Tokushima University 徳島大学 教育研究者総覧
岩浅, 亮彦 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
市原, 亜起 Tokushima University
天眞, 寛文 Tokushima University 徳島大学 教育研究者総覧
渡邉, 佳一郎 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
日浅, 雅博 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
橋本, 一郎 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
田中, 栄二 Tokushima University|King Abdulaziz University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
Le Fort III osteotomy
Maxillary growth deficiency
Aim and objective: To present an Apert syndrome patient with midfacial growth deficiency treated with Le Fort III distraction osteogenesis and subsequent two-jaw surgery.
Background: Apert syndrome is expressed as a severe and irregular craniosynostosis, midfacial hypoplasia, and symmetric syndactyly in the fingers and toes. For craniosynostosis syndromes, treatment planning is complex due to the disharmony between facial profile and occlusion.
Case description: A 4-year-and-5-month-old boy, diagnosed with Apert syndrome, showed a concave profile accompanied with midfacial hypoplasia, moderate exorbitism, a reversed occlusion of −10.0 mm, an anterior open bite of −5.0 mm, and skeletal class III jaw-base relationship. The patient, aged 15 years and 4 months, underwent a Le Fort III osteotomy, and subsequent osteodistraction was performed via a rigid external distraction (RED) device. His midfacial bone was advanced by approximately 7.0 mm. One year after the distraction, preoperative treatment with 0.018-in preadjusted edgewise appliances was initiated. Two-jaw surgery with a Le Fort I osteotomy and bilateral sagittal split ramus osteotomy was performed after 42 months of preoperative orthodontic treatment. At the age of 20 years and 9 months, his facial profile dramatically changed to a straight profile, and an acceptable occlusion with an adequate interincisal relationship was obtained. A functional occlusion with an excellent facial profile was maintained throughout the 2-year retention period, although the upper dental arch width was slightly decreased, resulting in the recurrence of the left posterior crossbite.
Conclusion: Our report indicates the necessity of long-term follow-up in patients with craniosynostosis because of syndrome-specific growth and methodologically induced relapse.
Clinical significance: The two-stage operation combining early distraction osteogenesis and postgrowth orthognathic surgery proves to be an effective therapy for correcting midfacial hypoplasia and skeletal mandibular protrusion caused by Apert syndrome.
The Journal of Contemporary Dental Practice
Jaypee Brothers Medical Publishers
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