Lazebnik N, McPherson E, Rittmeyer L J, Mulvihill J J
Department of Genetics, Magee-Womens Hospital, Pittsburgh, PA 15213, USA.
Am J Med Genet. 1996 Dec 18;66(3):300-2. doi: 10.1002/(SICI)1096-8628(19961218)66:3<300::AID-AJMG12>3.0.CO;2-Q.
The Floating Harbor syndrome of short stature, very delayed bone age, expressive language delay, and characteristic facial changes has not been associated with cardiac anomalies, except for one patient with pulmonic stenosis. We report on a 10-year-old boy with the syndrome and tetralogy of Fallot with atrial septal defect.
弗洛廷港综合征表现为身材矮小、骨龄严重延迟、表达性语言发育迟缓及特征性面部改变，除1例患有肺动脉狭窄的患者外，尚未发现与心脏异常有关。我们报告1例患有该综合征并伴有房间隔缺损的法洛四联症的10岁男孩。
