Hodgson S V, Barber J C, Dowie A, Dubowitz V
J Med Genet. 1986 Oct;23(5):477-8. doi: 10.1136/jmg.23.5.477.
We describe a female infant who presented with hypotonia and developmental delay. Her karyotype showed a de novo balanced translocation between the X chromosome and chromosome 13, with breakpoints at Xq13 and 13p11. The normal X was late replicating in all cells examined. The cause of this patient's abnormal phenotype is discussed.
我们描述了一名患有肌张力减退和发育迟缓的女婴。她的核型显示X染色体与13号染色体之间存在新发的平衡易位,断点位于Xq13和13p11。在所有检查的细胞中,正常的X染色体复制较晚。本文讨论了该患者异常表型的原因。