Clementi M, Tenconi R, Turolla L, Silvan C, Bortotto L, Artifoni L
Dipartimento di Pediatria, Università di Padova, Italy.
Am J Med Genet. 1991 Nov 1;41(2):246-50. doi: 10.1002/ajmg.1320410223.
This report concerns 2 unrelated patients with apparent CHARGE association and a chromosome abnormality, resulting from different unbalanced familial translocations involving chromosomes 2 and 18 in one family, and chromosomes 3 and 22 in the other. Although the identification of two different chromosome abnormalities might be due to chance, the observation of a long arm deletion of chromosome 22 in patients 2 and of the frequent coexistence of CHARGE association and DiGeorge anomaly raise the possibility of a contiguous gene syndrome in at least some CHARGE cases.
本报告涉及2例无亲缘关系的患者,他们患有明显的CHARGE综合征并伴有染色体异常。其中一个家族的异常是由涉及2号和18号染色体的不同不平衡家族性易位导致,另一个家族则是由涉及3号和22号染色体的不平衡家族性易位所致。虽然发现两种不同的染色体异常可能是巧合,但在患者2中观察到22号染色体长臂缺失,以及CHARGE综合征与迪格奥尔格综合征常同时出现,这提示至少在部分CHARGE综合征病例中可能存在相邻基因综合征。