候选基因阻塞性睡眠呼吸暂停在非综合征的儿童面形 - - 一个叙事审查
Zuzana Marincak Vrankova1,2,3, Jan Krivanek4, Zdenek Danek2,3
1Clinic of Stomatology, Institution Shared with St. Anne's University Hospital, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Frontiers in pediatrics
|July 13, 2023
概括
面遗传因素可能导致儿科阻塞性睡眠呼吸暂停 (POSA). 本综述确定了POSA的候选基因,将面发育与这种常见的儿童睡眠障碍联系起来.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 睡眠医学 睡眠医学
背景情况:
- 儿科阻塞性睡眠呼吸暂停 (POSA) 是一种由上呼吸道通透度影响的复杂疾病.
- 面形障碍,如逆转形和中面形,是POSA的危险因素.
- 这些特征具有很高的遗传性,并且可以在POSA的非综合征儿童中发生.
研究的目的:
- 探索儿童POSA的遗传基础,特别是关于面发育的遗传基础.
- 确定与可能使儿童易患POSA的面特征相关的候选基因.
- 审查高POSA患病率综合征中的遗传因素及其与非综合征病例的相关性.
主要方法:
- 叙述综合征的综合征与面形和睡眠相关呼吸障碍 (SRBD) 相关的叙述审查.
- 这些综合征的遗传背景的总结.
- 鉴定与面发育相关的POSA候选基因.
主要成果:
- 提出了30个对影响面发育的POSA候选基因.
- 其中七个基因以前与面特征有关,在非综合征儿童中增加POSA风险.
- 有证据表明,这些基因可能会在综合征和非综合征儿科群体中导致POSA.
结论:
- 影响面发育的遗传变异是POSA的潜在贡献者.
- 已发现的候选基因在一般儿科患者群体中需要进一步调查.
- 了解这些遗传联系可以促进对POSA病因和治疗的研究.
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