Kelley R I, Zackai E H, Emanuel B S, Kistenmacher M, Greenberg F, Punnett H H
J Pediatr. 1982 Aug;101(2):197-200. doi: 10.1016/s0022-3476(82)80116-9.
We have seen three unrelated patients with the DiGeorge anomalad who also had the same deletion of chromosome 22 (pter leads to qll). In each, the remaining long arm material (qll leads to qter) was translocated to a different autosome. Our patients and a review of the literature, including a recent report of a family having four infants with the DiGeorge anomalad and the same deletion of chromosome 22 (de la Chapelle et al: Hum Genet 57:253, 1981), make a strong argument for at least some cases of the DiGeorge anomalad arising from a deletion of the pericentromeric region of chromosome 22.
我们见过3例患有迪格奥尔格综合征异常的无血缘关系患者,他们都有相同的22号染色体缺失(从pter到qll)。在每例患者中,剩余的长臂物质(从qll到qter)都易位到了一条不同的常染色体上。我们的患者以及对文献的回顾,包括最近一篇关于一个家庭中有4名患有迪格奥尔格综合征异常且有相同22号染色体缺失的婴儿的报告(德拉沙佩勒等人:《人类遗传学》57:253,1981),有力地证明了至少部分迪格奥尔格综合征异常病例是由22号染色体着丝粒周围区域的缺失引起的。