Catch-Up Growth in Syndromic Robin Sequence: A Systematic Review.

IF 1.3 4区 医学 Q2 Dentistry
Cleft Palate-Craniofacial Journal Pub Date : 2026-10-01 Epub Date: 2025-11-18 DOI:10.1177/10556656251392267
Sogand Schafer, Jason Yu, John B Mulliken
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引用次数: 0

Abstract

ObjectiveThe triad of micrognathia, glossoptosis, and airway obstruction defines Robin sequence (RS). Syndromic RS accounts for about 60% of cases, but whether mandibular "catch-up" growth occurs in these cases remains unclear. The aim of the systematic review was to assess the current literature for evidence of catch-up growth in syndromic RS.DesignA PRISMA-guided systematic literature review was performed. PubMed was searched for studies describing cases with syndromic RS who underwent conservative (non-surgical) management.Patients, ParticipantsCase reports, case series, and chart reviews containing both the diagnosis of RS and at least one associated syndrome were included. Review articles, non-English publications, and studies lacking sufficient follow-up or clarity on mandibular morphology were excluded.Main Outcome MeasuresThe review assessed micrognathia, mandibular length, catch-up growth, and the necessity of airway enhancement.ResultsThirty-four studies met the criteria for inclusion. These studies included clinical information from a total of 202 cases and addressed 20 different syndromes. RS in the context of Stickler syndrome and 22q11.2 deletion syndrome were most frequently reported, with multiple studies suggesting potential for balanced maxillo-mandibular growth or apparent catch-up growth. However, definitive conclusions were limited by small study population, heterogeneous methodologies, and variable follow-up durations.ConclusionWhile additional data are needed, available literature suggests that certain syndromic RS groups may exhibit spontaneous mandibular growth, potentially reducing the need for invasive procedures such as distraction osteogenesis. Prospective research employing standardized cephalometric measures is necessary to identify which syndromic subpopulations and RS types benefit from conservative versus surgical management.

综合征Robin序列的赶超生长:系统综述。
目的以小颌、舌下垂、气道梗阻三联征定义Robin序列。综合征型RS约占60%的病例,但在这些病例中是否发生下颌“追赶”生长尚不清楚。系统回顾的目的是评估当前文献中综合征rs的追赶性增长证据。designa prisma引导的系统文献回顾进行。PubMed检索了描述综合征性RS患者接受保守(非手术)治疗的研究。纳入了包括RS诊断和至少一种相关综合征的患者、参与者病例报告、病例系列和图表回顾。综述性文章、非英文出版物和缺乏足够随访或下颌形态学清晰度的研究被排除在外。主要观察指标:该综述评估了小颌、下颌长度、追赶生长和气道增强的必要性。结果34项研究符合纳入标准。这些研究包括202例病例的临床信息,涉及20种不同的综合征。在Stickler综合征和22q11.2缺失综合征的背景下,RS最常被报道,多项研究表明可能存在平衡的上颌-下颌生长或明显的追赶生长。然而,明确的结论受到研究人群小、方法异质性和随访时间变化的限制。结论虽然需要更多的数据,但现有文献表明,某些综合征RS组可能表现出自发的下颌生长,潜在地减少了对牵张成骨等侵入性手术的需求。采用标准化头颅测量的前瞻性研究是必要的,以确定哪些综合征亚群和RS类型从保守治疗和手术治疗中受益。
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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来源期刊
Cleft Palate-Craniofacial Journal
Cleft Palate-Craniofacial Journal DENTISTRY, ORAL SURGERY & MEDICINE-SURGERY
CiteScore
2.20
自引率
36.40%
发文量
0
审稿时长
4-8 weeks
期刊介绍: The Cleft Palate-Craniofacial Journal (CPCJ) is the premiere peer-reviewed, interdisciplinary, international journal dedicated to current research on etiology, prevention, diagnosis, and treatment in all areas pertaining to craniofacial anomalies. CPCJ reports on basic science and clinical research aimed at better elucidating the pathogenesis, pathology, and optimal methods of treatment of cleft and craniofacial anomalies. The journal strives to foster communication and cooperation among professionals from all specialties.
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