Research Review of Myhre Syndrome.

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY
Maggie R Brand, Ryan Monsberger, Robert J Hopkin, Angela E Lin
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引用次数: 0

Abstract

This research review of Myhre syndrome is a summary of published articles which provide a valuable resource for readers, researchers, and future authors. It traces the evolution of the Laryngotracheal-Arthropathy-Prognathism-Short Stature (LAPS) syndrome to the current eponym of Myhre syndrome. These allelic disorders are caused by pathogenic variants in SMAD4. After the initial report over 40 years ago, the steady publication of case reports and small series was accelerated following the discovery of the pathogenic variants in SMAD4. The articles in this review include numerous case reports and small series, reports about basic science, the discovery of the causative gene, the emergence of the natural history in larger studies, and articles about specific features, especially the cardiovascular system and airways. We hope this analysis provides a foundation for future research that may extend symptom-based treatment to genetic-based therapy.

Myhre综合征的研究综述。
这篇关于Myhre综合征的研究综述是对已发表文章的总结,为读者、研究人员和未来的作者提供了宝贵的资源。它追溯了喉气管-关节病-前突-身材矮小(LAPS)综合征的演变到现在的Myhre综合征。这些等位基因疾病是由SMAD4的致病变异引起的。在40多年前的首次报告之后,随着SMAD4致病变异的发现,病例报告和小系列的稳步出版加快了。这篇综述中的文章包括大量的病例报告和小系列,关于基础科学的报告,致病基因的发现,自然历史在大型研究中的出现,以及关于特定特征的文章,特别是心血管系统和气道。我们希望这一分析能为未来的研究提供基础,将基于症状的治疗扩展到基于基因的治疗。
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
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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