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牙齿异常的人类遗传学

The Human Genetics of Dental Anomalies.

作者信息

Khan Mahamad Irfanulla, Ahmed Nadeem, Neela Praveen Kumar, Unnisa Nayeem

机构信息

Department of Orthodontics & Dentofacial Orthopedics, The Oxford Dental College, Bangalore, Karnataka, India.

General Dental Practitioner, Max Dental Specialties, Bangalore, Karnataka, India.

出版信息

Glob Med Genet. 2022 Feb 25;9(2):76-81. doi: 10.1055/s-0042-1743572. eCollection 2022 Jun.


DOI:10.1055/s-0042-1743572
PMID:35707781
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9192175/
Abstract

The development of tooth is a highly complex procedure and mastered by specific genetic programs. Genetic alterations, environmental factors, and developmental timing can disturb the execution of these programs, and result in various dental anomalies like hypodontia/oligodontia, and supernumerary teeth, which are commonly seen in our clinical practice. Advances in molecular research enabled the identification of various genes involved in the pathogenesis of dental anomalies. In the near future, it will help provide a more accurate diagnosis and biological-based treatment for these anomalies. In this article, we present the molecular phenomenon of tooth development and the genetics of various dental anomalies.

摘要

牙齿发育是一个高度复杂的过程,由特定的基因程序控制。基因改变、环境因素和发育时机都会干扰这些程序的执行,导致各种牙齿异常,如牙缺失/少牙症和多生牙,这些在我们的临床实践中很常见。分子研究的进展使得人们能够识别出参与牙齿异常发病机制的各种基因。在不久的将来,它将有助于为这些异常提供更准确的诊断和基于生物学的治疗方法。在本文中,我们介绍了牙齿发育的分子现象以及各种牙齿异常的遗传学。

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本文引用的文献

[1]
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BDJ Open. 2021-7-9

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Am J Med Genet A. 2019-8-29

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