13-染色体缺失综合征合并视网膜母细胞瘤一例_Chinese Journal of Ocular Fundus Diseases

Authors：

要青清 , 程湧 , 令狐丹丹 , 朱雪梅 , 邓洵 ,  梁建宏

北京大学人民医院眼科 100044;
要青清，现在邯郸市第一医院眼科 056002;

Corresponding author：

梁建宏, Email: drliangjianhong@126.com

Keywords：

染色体缺失; 视网膜母细胞瘤; 病例报告

DOI：

10.3760/cma.j.cn511434-20190711-00221

Video：

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Citation： 要青清, 程湧, 令狐丹丹, 朱雪梅, 邓洵, 梁建宏. 13-染色体缺失综合征合并视网膜母细胞瘤一例. Chinese Journal of Ocular Fundus Diseases, 2020, 36(10): 804-805. doi: 10.3760/cma.j.cn511434-20190711-00221 Copy

1.	Kirchhoff M, Bisgaard AM, Stoeva R, et al. Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter[J]. Am J Med Genet A, 2009, 149A(5): 894-905. DOI: 10.1002/ajmg.a.32814.
2.	Lévy J, Haye D, Marziliano N, et al. EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder[J]. Clin Genet, 2018, 93(6): 1141-1147. DOI: 10.1111/cge.13234.
3.	Jones K, Minassian BA. Genetic testing in infantile spasms identifies a chromosome 13q deletion and retinoblastoma[J]. Pediatr Neurol, 2014, 50(5): 522-524. DOI: 10.1016/j.pediatrneurol.2013.11.018.
4.	Abramson DH, Shield CL, Munier FL, et al. Treatment of retinoblastoma in 2015: agreement and disagreement[J]. JAMA Ophthalmol, 2015, 133(11): 1341-1347. DOI: 10.1001/Jamaophthalmol.2015.3108.

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Chinese Journal of Ocular Fundus Diseases

13-染色体缺失综合征合并视网膜母细胞瘤一例

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