Naguib K K, Hamoud M S, Khalil E S, el-Khalifa M Y
Kuwait Medical Genetics Centre, Maternity Hospital, Safat.
J Med Genet. 1991 Feb;28(2):138-9. doi: 10.1136/jmg.28.2.138.
We describe a newborn Arab male with defects similar to those seen in mice heterozygous for the mutant disorganisation (DS) gene. He had complete absence of the left lower limb including the left pelvic bone, hamartomas arising from the abdominal wall, a small penis, absent left half of the scrotal sac, absent left testicle, anterior displacement of the anus, and multiple vertebral defects. The similarity between the proband's anomalies and those found in affected heterozygotes for DS support the possibility of a human homologue of the DS gene.
我们描述了一名新生阿拉伯男性,其缺陷与突变的无序(DS)基因杂合子小鼠中所见的缺陷相似。他完全没有左下肢,包括左髋骨,腹壁出现错构瘤,阴茎短小,阴囊囊左侧缺失,左睾丸缺失,肛门向前移位,以及多处脊椎缺陷。先证者的异常与DS基因杂合子患者中发现的异常之间的相似性支持了存在DS基因人类同源物的可能性。