| Literature DB >> 29928183 |
Marta-Catalina Miranda-Fernández1, Silvia Ramírez-Oyaga1, Carlos M Restrepo2, Victor-Manuel Huertas-Quiñones3,4,5, Magally Barrera-Castañeda6, Rossi Quero2, Camilo-José Hernández-Toro1, Claudia Tamar Silva2, Paul Laissue2, Rodrigo Cabrera1.
Abstract
Ebstein anomaly (EA) is a rare congenital heart defect (CHD) with a poorly characterized genetic etiology. However, some EA patients carry deletions in 1p36, all of which have been reported to carry distal deletions and share loss of the PRDM16 gene, which is currently considered the most likely candidate for EA development in this region. Here, we report a patient with an 11.96-Mb proximal 1p36 deletion, without loss of PRDM16, who presented with EA and a proximal deletion phenotype. This finding suggests that PRDM16 loss is not required for the development of EA in 1p36 deletions and that the loss of an additional proximal locus in 1p36 is also likely associated with EA. Our data suggest that a distal locus containing the SKI gene and a proximal locus containing the CHD-associated genes RERE and UBE4B are the most probable etiological factors for EA in patients with 1p36 deletion syndrome.Entities:
Keywords: 1p36 deletion syndrome; Ebstein anomaly; PRDM16; RERE; SKI; UBE4B
Year: 2018 PMID: 29928183 PMCID: PMC6006643 DOI: 10.1159/000488820
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769