Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12


  • Markus Draaken, Sadaf S. Mughal, Tracie Pennimpede, Lars Wittler, Anne-Karoline Ebert, Wolfgang Rösch, Raimund Stein, Enrika Bartels, Dominik Schmidt, Thomas M. Boemers, Eberhard Schmiedeke, Per Hoffmann, Bernhard G. Herrmann, Markus M. Nöthen, Heiko Reutter, and Michael Ludwig are members of the “Network for the Systematic Investigation of the Molecular Causes, Clinical Implications and Psychosocial Outcome of Congenital Uro-Rectal Malformations (CURE-Net)” which is supported by a research grant from the BMBF.

  • Supported by grant from the German Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung, BMBF; 01GM08107), the BONFOR program of the University of Bonn (O-149.0099 to EB), and the Richard-Winter-Stiftung (to SSM).



The exstrophy-epispadias complex (BEEC) is a urogenital birth defect of varying severity. The causes of the BEEC are likely to be heterogeneous, with individual environmental or genetic risk factors still being largely unknown. In this study, we aimed to identify de novo causative copy number variations (CNVs) that contribute to the BEEC.

METHODS Array-based molecular karyotyping was performed to screen 110 individuals with BEEC. Promising CNVs were tested for de novo occurrence by investigating parental DNAs. Genes located in regions of rearrangements were prioritized through expression analysis in mice to be sequenced in the complete cohort, to identify high-penetrance mutations involving small sequence changes. RESULTS A de novo 0.9 Mb microduplication involving chromosomal region 19p13.12 was identified in a single patient. This region harbors 20 validated RefSeq genes, and in situ hybridization data showed specific expression of the Wiz gene in regions surrounding the cloaca and the rectum between GD 9.5 and 13.5. Sanger sequencing of the complete cohort did not reveal any pathogenic alterations affecting the coding region of WIZ. CONCLUSIONS The present study suggests chromosomal region 19p13.12 as possibly involved in the development of CBE, but further studies are needed to prove a causal relation. The spatiotemporal expression patterns determined for the genes encompassed suggest a role for Wiz in the development of the phenotype. Our mutation screening, however, could not confirm that WIZ mutations are a frequent cause of CBE, although rare mutations might be detectable in larger patient samples.

19p13.12, microduplication, bladder exstrophy-epispadias complex, array-based molecular karyotyping, in situ hybridization analysis, copy number variations, WIZ Birth Defects Research (Part A), 2013. © 2013 Wiley Periodicals, Inc.