Abraham Mary B, Carpenter Karen, Baynam Gareth S, Mackay Deborah Jg, Price Glynis, Choong Catherine S
Department of Endocrinology and Diabetes, Princess Margaret Hospital for Children, Perth, Western Australia, Australia.
Department of Diagnostic Genomics, PathWest, QEII Medical Centre, Perth, Western Australia, Australia.
J Paediatr Child Health. 2015 May;51(5):555-560. doi: 10.1111/jpc.12778. Epub 2014 Nov 23.
Silver-Russell syndrome (SRS) and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome are described in isolation. However, their co-occurrence has only been rarely reported. Here, we present a case report of an adolescent with SRS who was diagnosed with MRKH during the evaluation of primary amenorrhoea. Multiplex ligation-dependent probe amplification analysis showed a normal methylation pattern and normal dosage at 11p15.5. A PubMed search for all peer-reviewed publications (original articles and reviews) using the key words Silver-Russell syndrome, Mayer-Rokitansky-Küster-Hauser syndrome, genetics, hypomethylation and reproductive anomalies identified three cases of SRS with MRKH, two of which were associated with significant hypomethylation of the H19 imprinting control region of the 11p15.5 locus. This report highlights the association between SRS and MRKH. The absence of hypomethylation and normal dosage at 11p15.5 suggests these two rare entities share alternative aetiopathogenic mechanisms.
Silver-Russell综合征(SRS)和Mayer-Rokitansky-Küster-Hauser综合征(MRKH)通常分别被描述。然而,它们同时出现的情况鲜有报道。在此,我们报告一例患有SRS的青少年病例,该患者在原发性闭经评估过程中被诊断出患有MRKH。多重连接依赖探针扩增分析显示11p15.5处甲基化模式正常且剂量正常。通过在PubMed上使用关键词Silver-Russell综合征、Mayer-Rokitansky-Küster-Hauser综合征、遗传学、低甲基化和生殖异常搜索所有同行评审出版物(原创文章和综述),发现了3例SRS合并MRKH的病例,其中两例与11p15.5位点H19印记控制区域的显著低甲基化有关。本报告强调了SRS与MRKH之间的关联。11p15.5处无低甲基化且剂量正常表明这两种罕见病症具有不同的病因致病机制。