Stevens C A, Fineman R M, Breg W R, Silken A B
Department of Pediatrics, University of Utah School of Medicine, Salt Lake City 84132.
Am J Med Genet. 1988 Apr;29(4):807-14. doi: 10.1002/ajmg.1320290410.
We report on two patients with distal deletions of 6q. In one case a de novo translocation between chromosomes 6 and 7 resulted in del(6q25----6qter). The other case had a de novo deletion, also from 6q25 to 6qter. There have been eight previous reports of distal deletions of 6q. These patients have developmental retardation, microcephaly, craniofacial anomalies, various types of congenital heart defects, and anomalies of hands and feet. The facial similarities of our two patients and those in six published photographs are subtle and may represent an emerging phenotype.
我们报告了两名6号染色体长臂远端缺失的患者。其中一例6号和7号染色体之间的新发易位导致了6q25至6q末端的缺失。另一例也是新发缺失,同样是从6q25至6q末端。此前已有8例6号染色体长臂远端缺失的报告。这些患者有发育迟缓、小头畸形、颅面异常、各种类型的先天性心脏缺陷以及手足异常。我们两名患者与六张已发表照片中的患者面部相似之处不明显,可能代表一种新出现的表型。