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非综合征型唇裂伴或不伴腭裂的遗传继承模型:从单基因到多基因。

Genetic Inheritance Models of Non-Syndromic Cleft Lip with or without Palate: From Monogenic to Polygenic.

机构信息

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.

Department of Plastic Surgery, Peking Union Medical College Hospital, Beijing 100730, China.

出版信息

Genes (Basel). 2023 Sep 24;14(10):1859. doi: 10.3390/genes14101859.

Abstract

Non-syndromic cleft lip with or without palate (NSCL/P) is a prevalent birth defect that affects 1/500-1/1400 live births globally. The genetic basis of NSCL/P is intricate and involves both genetic and environmental factors. In the past few years, various genetic inheritance models have been proposed to elucidate the underlying mechanisms of NSCL/P. These models range from simple monogenic inheritance to more complex polygenic inheritance. Here, we present a comprehensive overview of the genetic inheritance model of NSCL/P exemplified by representative genes and regions from both monogenic and polygenic perspectives. We also summarize existing association studies and corresponding loci of NSCL/P within the Chinese population and highlight the potential of utilizing polygenic risk scores for risk stratification of NSCL/P. The potential application of polygenic models offers promising avenues for improved risk assessment and personalized approaches in the prevention and management of NSCL/P individuals.

摘要

非综合征性唇裂伴或不伴腭裂(NSCL/P)是一种常见的出生缺陷,全球每 500-1400 例活产中就有 1 例。NSCL/P 的遗传基础复杂,涉及遗传和环境因素。在过去的几年中,已经提出了各种遗传遗传模型来阐明 NSCL/P 的潜在机制。这些模型从简单的单基因遗传到更复杂的多基因遗传不等。在这里,我们从单基因和多基因的角度,通过代表性基因和区域,全面概述了 NSCL/P 的遗传遗传模型。我们还总结了中国人群中 NSCL/P 的现有关联研究和相应位点,并强调了利用多基因风险评分对 NSCL/P 进行风险分层的潜力。多基因模型的潜在应用为改善 NSCL/P 个体的风险评估和个性化预防管理提供了有希望的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a5a/10606748/36253dfbeaf1/genes-14-01859-g001.jpg

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