影响 Silver-Russell 综合征 HMGA2 的致病序列变异和微缺失:病例报告和文献综述。

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY
Kaori Yamoto, Hirotomo Saitsu, Yumiko Ohkubo, Masayo Kagami, Tsutomu Ogata
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引用次数: 0

摘要

西尔弗-鲁塞尔综合征(SRS)是一种具有代表性的印记障碍疾病,其特征是出生前后发育不良。我们在日本发现了两例 SRS 患者,他们分别患有 HMGA2(NM_003483.6:c.138_141delinsCT, p.(Lys46Asnfs*16))的从头致病性框移变异和涉及 HMGA2 的 12q14.2-q15 的从头 ~ 3.4 Mb 微缺失。此外,我们还比较了以前报道过的导致 IGF2 表达受损的各种遗传病患者的临床特征,即 HMGA2 畸变、PLAG1 畸变、IGF2 畸变和 H19/IGF2:IG-DMR 外显子(低甲基化)。这些结果进一步支持了HMGA2参与SRS的发病,并暗示了HMGA2畸变患者的一些特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver-Russell syndrome: case reports and literature review.

Silver-Russell syndrome (SRS) is a representative imprinting disorder characterized by pre- and postnatal growth failure. We encountered two Japanese SRS cases with a de novo pathogenic frameshift variant of HMGA2 (NM_003483.6:c.138_141delinsCT, p.(Lys46Asnfs*16)) and a de novo ~ 3.4 Mb microdeletion at 12q14.2-q15 involving HMGA2, respectively. Furthermore, we compared clinical features in previously reported patients with various genetic conditions leading to compromised IGF2 expression, i.e., HMGA2 aberrations, PLAG1 aberrations, IGF2 aberrations, and H19/IGF2:IG-DMR epimutations (hypomethylations). The results provide further support for HMGA2 being involved in the development of SRS and imply some characteristic features in patients with HMGA2 aberrations.

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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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