Department of Biochemistry, Hamamatsu University School of Medicine, 1-20-1, Handayama, Chuo-ku, Hamamatsu, 431-3192, Japan.
Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Clin Epigenetics. 2024 Jun 5;16(1):73. doi: 10.1186/s13148-024-01688-w.
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.
银-罗素综合征(SRS)是一种代表性的印迹障碍,其特征是产前和产后生长发育不良。我们遇到了两个日本 SRS 病例,分别存在 HMGA2 的从头致病性移码变异(NM_003483.6:c.138_141delinsCT,p.(Lys46Asnfs*16))和 12q14.2-q15 处涉及 HMGA2 的从头~3.4 Mb 微缺失。此外,我们比较了先前报道的各种导致 IGF2 表达受损的遗传条件(即 HMGA2 异常、PLAG1 异常、IGF2 异常和 H19/IGF2:IG-DMR 表观突变(低甲基化))患者的临床特征。结果进一步支持 HMGA2 参与 SRS 的发生,并暗示 HMGA2 异常患者具有一些特征性表现。