New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.

Published

Journal Article

Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome demonstrating heterogeneous molecular alterations of two imprinted domains on chromosome 11p15. The most common molecular alterations include loss of methylation at the proximal imprinting center, IC2, paternal uniparental disomy (UPD) of chromosome 11p15 and hypermethylation at the distal imprinting center, IC1. An increased incidence of female monozygotic twins discordant for BWS has been reported. The molecular basis for eleven such female twin pairs has been demonstrated to be a loss of methylation at IC2, whereas only one male monozygotic twin pair has been reported with this molecular defect. We report here two new pairs of male monozygotic twins. One pair is discordant for BWS; the affected twin exhibits paternal UPD for chromosome 11p15 whereas the unaffected twin does not. The second male twin pair is concordant for BWS and both twins of the pair demonstrate hypermethylation at IC1. Thus, this report expands the known molecular etiologies for BWS twins. Interestingly, these findings demonstrate a new epigenotype-phenotype correlation in BWS twins. That is, while female monozygotic twins with BWS are likely to show loss of imprinting at IC2, male monozygotic twins with BWS reflect the molecular heterogeneity seen in BWS singletons. These data underscore the need for molecular testing in BWS twins, especially in view of the known differences among 11p15 epigenotypes with respect to tumor risk.

Full Text

Duke Authors

Cited Authors

  • Smith, AC; Rubin, T; Shuman, C; Estabrooks, L; Aylsworth, AS; McDonald, MT; Steele, L; Ray, PN; Weksberg, R

Published Date

  • 2006

Published In

Volume / Issue

  • 113 / 1-4

Start / End Page

  • 313 - 317

PubMed ID

  • 16575195

Pubmed Central ID

  • 16575195

Electronic International Standard Serial Number (EISSN)

  • 1424-859X

Digital Object Identifier (DOI)

  • 10.1159/000090847

Language

  • eng

Conference Location

  • Switzerland