Report and review of described associations of Mayer‐Rokitansky‐Küster‐Hauser syndrome and Silver–Russell syndrome. (23rd November 2014)

• Record Type: Journal Article
• Authors: Abraham, Mary B; Carpenter, Karen; Baynam, Gareth S; Mackay, Deborah JG; Price, Glynis; Choong, Catherine S
• Is Part Of: Journal of paediatrics and child health. Volume 51:Number 5(2015:May)
• Page Start: 555
• Page End: 560
• Publication Date: 2014-11-23
• Subjects: Children -- Health and hygiene -- Periodicals; Pediatrics -- Periodicals; 618.92
• DOI: 10.1111/jpc.12778
• Languages: English
• ISSNs: 1034-4810

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <p>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.</p> </abstract>