Duplication of 19q (13.2-13.31) associated with comitant esotropia: A case report

doi:10.12998/wjcc.v9.i20.5526

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World Journal of Clinical Cases

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Jul 16, 2021; 9(20): 5526-5534
Published online Jul 16, 2021. doi: 10.12998/wjcc.v9.i20.5526

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Figure 5 Genomic coordinates for the 19q13. 2-q13.31 gain are chr19:39,343,725-43,762,586 (hg38), estimated to be 4.42 Mb. This duplication includes 27 OMIM Morbid genes: Plekhg2, Timm50, Dll3, Dyrk1b, Akt2, Pld3, Prx, Sptbn4, Ltbp4, Coq8b, Itpkc, Cyp2a4, Cyp2a5, Cyp2b10, Tgfb1, B9d2, Bckdha, Rps19, Cd79a, Atp1a3, Erf, Cic, Megf8, Lipe, Ethe1, Xrcc1, and Smg9 (hg38 database, http://genome.ucsc.edu).

Citation: Feng YL, Li ND. Duplication of 19q (13.2-13.31) associated with comitant esotropia: A case report. World J Clin Cases 2021; 9(20): 5526-5534
URL: https://www.wjgnet.com/2307-8960/full/v9/i20/5526.htm
DOI: https://dx.doi.org/10.12998/wjcc.v9.i20.5526