A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith–Wiedemann or Silver–Russell syndrome in a single family. Issue 1 (9th September 2016)

• Record Type: Journal Article
• Authors: Jurkiewicz, Dorota; Kugaudo, Monika; Skórka, Agata; Śmigiel, Robert; Smyk, Marta; Ciara, Elżbieta; Chrzanowska, Krystyna; Krajewska‐Walasek, Małgorzata
• Is Part Of: American journal of medical genetics. Volume 173:Issue 1(2017)
• Page Start: 72
• Page End: 78
• Publication Date: 2016-09-09
• Subjects: Beckwith–Wiedemann syndrome -- Silver–Russell syndrome -- 11p15.5 imprinting region -- IGF2/H19 domain triplication; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.37964
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract : Defects of 11p15.5 imprinting result in two growth disorders with opposite phenotypes: Beckwith–Wiedemann syndrome (BWS) characterized by overgrowth and Silver–Russell syndrome (SRS) associated with growth retardation. In a small group of patients with BWS and SRS, copy number variations (CNVs) involving the 11p15.5 region are observed; and their effects depend on the localization, size, and the parental mode of transmission. We report a novel IGF2/H19 domain cis ‐triplication in the 11p15.5 region identified in a girl with BWS and her father with symptoms of SRS. To the best of our knowledge, this is the first report of IGF2/H19 domain triplication associated with BWS or SRS and the second report of an additional copy of this region in an individual with clinical features of SRS. This study shows that paternal IGF2/H19 domain triplication results in BWS, gives additional support to the hypothesis that the maternal amplification of IGF2/H19 domain may lead to the manifestation of SRS and underlines difficulties of genetic counseling in patients with CNVs involving the 11p15.5 region. © 2016 Wiley Periodicals, Inc.