TY - JOUR T1 - Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size JF - Journal of Medical Genetics JO - J Med Genet SP - 332 LP - 341 DO - 10.1136/jmg.2009.073015 VL - 47 IS - 5 AU - Marwan Shinawi AU - Pengfei Liu AU - Sung-Hae L Kang AU - Joseph Shen AU - John W Belmont AU - Daryl A Scott AU - Frank J Probst AU - William J Craigen AU - Brett H Graham AU - Amber Pursley AU - Gary Clark AU - Jennifer Lee AU - Monica Proud AU - Amber Stocco AU - Diana L Rodriguez AU - Beth A Kozel AU - Steven Sparagana AU - Elizabeth R Roeder AU - Susan G McGrew AU - Thaddeus W Kurczynski AU - Leslie J Allison AU - Stephen Amato AU - Sarah Savage AU - Ankita Patel AU - Pawel Stankiewicz AU - Arthur L Beaudet AU - Sau Wai Cheung AU - James R Lupski Y1 - 2010/05/01 UR - http://jmg.bmj.com/content/47/5/332.abstract N2 - Background Deletion and the reciprocal duplication in 16p11.2 were recently associated with autism and developmental delay.Method We indentified 27 deletions and 18 duplications of 16p11.2 were identified in 0.6% of all samples submitted for clinical array-CGH (comparative genomic hybridisation) analysis. Detailed molecular and phenotypic characterisations were performed on 17 deletion subjects and ten subjects with the duplication.Results The most common clinical manifestations in 17 deletion and 10 duplication subjects were speech/language delay and cognitive impairment. Other phenotypes in the deletion patients included motor delay (50%), seizures (∼40%), behavioural problems (∼40%), congenital anomalies (∼30%), and autism (∼20%). The phenotypes among duplication patients included motor delay (6/10), behavioural problems (especially attention deficit hyperactivity disorder (ADHD)) (6/10), congenital anomalies (5/10), and seizures (3/10). Patients with the 16p11.2 deletion had statistically significant macrocephaly (p<0.0017) and 6 of the 10 patients with the duplication had microcephaly. One subject with the deletion was asymptomatic and another with the duplication had a normal cognitive and behavioural phenotype. Genomic analyses revealed additional complexity to the 16p11.2 region with mechanistic implications. The chromosomal rearrangement was de novo in all but 2 of the 10 deletion cases in which parental studies were available. Additionally, 2 de novo cases were apparently mosaic for the deletion in the analysed blood sample. Three de novo and 2 inherited cases were observed in the 5 of 10 duplication patients where data were available.Conclusions Recurrent reciprocal 16p11.2 deletion and duplication are characterised by a spectrum of primarily neurocognitive phenotypes that are subject to incomplete penetrance and variable expressivity. The autism and macrocephaly observed with deletion and ADHD and microcephaly seen in duplication patients support a diametric model of autism spectrum and psychotic spectrum behavioural phenotypes in genomic sister disorders. ER -