National Genetic Centre, Royal Hospital, Ministry of Health, Muscat, Oman.
Sultan Qaboos Univ Med J. 2023 May;23(2):264-268. doi: 10.18295/squmj.4.2022.033. Epub 2023 May 31.
Silver-Russell Syndrome (SRS) is a disorder that is primarily characterised by intrauterine growth restriction which may occur asymmetrically or in whole, leading to a fetus being small relative to its gestational age. We present a female infant (proband) born in 2018 at a tertiary hospital in Muscat, Oman, with severe congenital anomalies. The proband carried a >25Mb duplication of the chromosomal 11p15-11pter locus of chromosome 13; creating a derivative chromosome 13 (der[13]) and was reported as 46,XX,der(13)add(11p15-11pter). A methylation-sensitive assay confirmed a diagnosis of SRS. Although the prognosis for SRS patients is generally good, the proband presented with a clinically severe phenotype culminating in death at the age of nine months. To the best of the authors' knowledge, this is the first report of a derivative chromosome 13 with a duplicated 11p15 locus in a patient with SRS.
银- Russell 综合征(SRS)是一种主要表现为宫内生长受限的疾病,其可能呈不对称性或整体性发生,导致胎儿相对于其胎龄较小。我们介绍了一名于 2018 年在阿曼马斯喀特的一家三级医院出生的女性婴儿(先证者),患有严重的先天性异常。先证者携带染色体 13 上 11p15-11pter 染色体区域的>25Mb 重复,形成衍生染色体 13(der[13]),并被报告为 46,XX,der(13)add(11p15-11pter)。一种甲基化敏感检测证实了 SRS 的诊断。尽管 SRS 患者的预后通常较好,但先证者表现出临床严重表型,最终在九个月大时死亡。据作者所知,这是首例报告的 SRS 患者携带 11p15 位点重复的衍生染色体 13。