TY - JOUR T1 - 20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits JF - Journal of Medical Genetics JO - J Med Genet DO - 10.1136/jmg.2008.061002 AU - Seema R Lalani AU - Joseph V Thakuria AU - Gerald F Cox AU - Xueqing Wang AU - Weimin Bi AU - Molly S Bray AU - Chad Shaw AU - Sau W Cheung AU - A Craig Chinault AU - Barbara A Boggs AU - Zhishuo Ou AU - Ellen K Brundage AU - James R Lupski AU - Jennifer Gentile AU - Susan Waisbren AU - Amber Pursley AU - Lijiang Ma AU - Mehrdad Khajavi AU - Gladys Zapata AU - Richard Friedman AU - Jeffrey J Kim AU - J A Towbin AU - Pawel Stankiewicz AU - Susanne Schnittger AU - Ingo Hansmann AU - Tomohiko Ai AU - Subeena Sood AU - Xander H Wehrens AU - James F Martin AU - John W Belmont AU - Lorraine Potocki Y1 - 2008/09/23 UR - http://jmg.bmj.com/content/early/2008/09/23/jmg.2008.061002.abstract N2 - Background: Wolff-Parkinson-White syndrome (WPW) is a bypass reentrant tachycardia that results from an abnormal connection between the atria and ventricles. Mutations in PRKAG2 have been described in patients with familial WPW syndrome and hypertrophic cardiomyopathy. Based on the role of bone morphogenetic protein (BMP) signaling in the development of annulus fibrosus in mice, it has been proposed that BMP signaling through the type 1a receptor and other downstream components may play a role in preexcitation. Methods and Results: Using the array comparative genomic hybridization (CGH), we identified five individuals with non-recurrent deletions of 20p12.3. Four of these individuals had WPW syndrome with variable dysmorphisms and neurocognitive delay. With the exception of one maternally inherited deletion, all occurred de novo, and the smallest of these, harbored a single gene, BMP2. In two individuals with additional features of Alagille syndrome, deletion of both JAG1 and BMP2 were identified. Deletion of this region has not been described as a copy-number variant in the Database of Genomic Variants and has not been identified in 13,321 individuals from other cohort examined by array CGH in our laboratory. Conclusions: Our findings demonstrate a novel genomic disorder characterized by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome. ER -