唇腭裂综合征患者的外显子组测序研究:系统综述。

IF 1.1 4区 医学 Q2 Dentistry
Diana Cárdenas-Nieto, Ignacio Briceño-Balcázar, Julio Martínez-Lozano, Milena Rondón-Lagos, Maribel Forero-Castro
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引用次数: 0

摘要

目的综合征型唇腭裂(CL/P)的病因是多因素和多基因的。本研究旨在确定外显子组测序诊断的遗传变异,并存在于这类患者中。DesignSystematic审查。方法根据PRISMA指南对PubMed数据库中的术语“腭裂”、“唇裂”、“唇腭裂”、“综合征”、“测序”和“外显子组”进行系统评价。患者和参与者包括综合征型CL/P患者。主要结果测量:外显子组测序诊断的患者存在遗传变异。结果共纳入19篇文献,其中41例患者共鉴定出62种变异。患者主要来自巴西(38.7%,24/62)、美国(11.3%,7/62)、中国(11.3%,7/62)、英国(9.7%,6/62)和亚洲(6.5%,4/62)。在变异方面,54个变异仅被发现一次,4个变异在不同的患者中被发现两次。受变异影响最大的基因为CHD7(4.8%, 3/62)、TP63(4.8%, 3/62)、MEIS2(6.5%, 4/62)和SATB2(6.5%, 4/62)。结论综合征型CL/P具有很大的表型变异性,难以将其与单一遗传原因或已知综合征联系起来。尽管在一些关键基因中发现了变异,但它们对胚胎发育的影响仍未完全了解。实施先进的基因组测序技术是提高患者诊断和临床护理的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exome Sequencing Studies in Syndromic Patients With Cleft Lip and/or Palate: Systematic Review.

ObjectiveThe etiology of syndromic cleft lip and/or cleft palate (CL/P) is multifactorial and polygenic. This study aims to identify genetic variants diagnosed by exome sequencing and present in this type of patients.DesignSystematic review.MethodsA systematic review was performed according to the PRISMA guidelines in the PubMed database including the terms "cleft palate," "cleft lip," "cleft lip and palate," "syndromic," "sequencing," and "exome."Patients and participantsPatients with syndromic CL/P were included.Main outcome measuresGenetic variants present in patients diagnosed by exome sequencing.ResultsA total of 19 articles were included, of which a total of 62 variants were identified in 41 patients. Patients were mainly from Brazil (38.7%, 24/62), the United States (11.3%, 7/62), China (11.3%, 7/62), the United Kingdom (9.7%, 6/62), and Asia (6.5%, 4/62). Regarding variants, 54 variants were identified only once and 4 variants were found twice in different patients. The genes most affected by the variants are: CHD7 (4.8%, 3/62), TP63 (4.8%, 3/62), MEIS2 (6.5%, 4/62), and SATB2 (6.5%, 4/62).ConclusionSyndromic CL/P presents a great phenotypic variability, which makes it difficult to associate it with a single genetic cause or known syndrome. Although variants have been identified in some key genes, their impact on embryonic development is still not fully understood. The implementation of advanced genomic sequencing techniques is key to improving diagnosis and clinical care of patients.

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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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