Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.

ABSTRACT:

Background

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth disorder associated with abnormalities in 11p15.5 imprinted genes. The most common cause is loss of methylation (epimutation) at the imprinting control centre 2 (IC2/KvDMR1). Most IC2 epimutations occur sporadically but an association with conception after assisted reproductive technologies (ART) has been reported. A subgroup of IC2 epimutation cases also harbour epimutations at other imprinting centres (ICs) outside of 11p15.5. We have investigated the relationship between these multiple epimutation cases (ME+), history of ART and clinical phenotype in a cohort of 187 BWS IC2 epimutation patients.

Results

Methylation analysis at PLAGL1, MEST and IGF2R ICs demonstrated an over-representation of patients

SUBMITTER: Tee L 

PROVIDER: S-EPMC3878854 | biostudies-literature | 2013 Dec

REPOSITORIES: biostudies-literature