Mandibular Distraction in Robin Sequence – A Systematic Review of Morphologic Changes and Implications for Long-Term Growth

FACE Pub Date : 2024-06-06 DOI:10.1177/27325016241255141
Hannes Prescher, Shelby L. Nathan, Kanad Ghosh, Charlotte Henderson, Russell R. Reid
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Abstract

Robin Sequence (RS) is a collection of distinct morphologic features involving the face and upper airway that results from the abnormal development of the neonatal mandible. Typically described as the triad of micrognathia, glossoptosis, and upper airway obstruction, it is frequently associated with a cleft palate and can be found in isolation or as part of a syndromic presentation. Owing to the intimate relationship between the mandible and its soft tissue attachments, micrognathia manifests clinically with respiratory and feeding difficulties. There is significant heterogeneity in both the degree of anatomic aberration and the associated physiological compromise, which dictates the medical and surgical treatment plan. In severe cases requiring surgical intervention, mandibular distraction osteogenesis (MDO) has been shown to be successful in relieving airway obstruction by correcting the morphologic deficiency of the mandible. However, controversy persists regarding the best treatment method as the exact relationship between the anatomic changes affected by MDO and the physiologic improvement remains poorly understood. This controversy is fueled by differing opinions about the natural growth potential of the abnormal mandible in patients with RS and the lack of long-term data on the maxillomandibular relationship at skeletal maturity of patients who underwent MDO in infancy. The objective of this systematic review is to provide a comprehensive summary of the morphologic changes to the mandible, upper airway, and hyoid bone affected by MDO and the impact of these changes on physiologic improvement and long-term growth.
罗宾序列中的下颌骨牵引--形态变化的系统回顾及其对长期生长的影响
罗宾序列(Robin Sequence,RS)是新生儿下颌骨发育异常导致的面部和上气道的一系列明显形态特征。通常被描述为小颌畸形、舌下垂和上气道阻塞三联征,经常与腭裂相关,可单独出现,也可作为综合征的一部分出现。由于下颌骨及其软组织附件之间的密切关系,小颌畸形在临床上表现为呼吸和喂养困难。小颌畸形的解剖畸变程度和相关的生理损害有很大的差异性,这决定了内外科治疗方案的不同。在需要手术干预的严重病例中,下颌骨牵引成骨术(MDO)已被证明可以通过矫正下颌骨的形态缺陷成功缓解气道阻塞。然而,关于最佳治疗方法的争议一直存在,因为人们对 MDO 所影响的解剖变化与生理改善之间的确切关系仍然知之甚少。由于对RS患者异常下颌骨的自然生长潜力存在不同看法,而且缺乏关于婴儿期接受MDO的患者骨骼成熟时上颌骨与下颌骨关系的长期数据,因此这种争议愈演愈烈。本系统综述旨在全面总结受 MDO 影响的下颌骨、上气道和舌骨的形态变化,以及这些变化对生理改善和长期生长的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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