Lai M M, Robards M F, Berry A C, Fear C N, Hart C
SE Thames Regional Genetic Centre, Guy's Hospital, London.
J Med Genet. 1991 Feb;28(2):128-30. doi: 10.1136/jmg.28.2.128.
We report two cases of interstitial deletion of the short arm of chromosome 1. The first was a 10 year old boy whose karyotype was 46,XY,del(1) (p22.1p31.2); the second was a 6 month old boy with a chromosome complement of 46,XY,del(1) (p22.3p31.3). A number of the malformations observed were common to both cases. There has been one previously reported case with the same breakpoints as our case 1 and a phenotype that was strikingly similar.
我们报告了两例1号染色体短臂间质性缺失的病例。第一例是一名10岁男孩,其核型为46,XY,del(1)(p22.1p31.2);第二例是一名6个月大的男孩,其染色体组成为46,XY,del(1)(p22.3p31.3)。两例中观察到的一些畸形是共有的。之前有一例报告的病例与我们的病例1具有相同的断点,且表型极为相似。