Goldberg R, Motzkin B, Marion R, Scambler P J, Shprintzen R J
Department of Plastic Surgery, Montefiore Medical Center, Bronx, NY 10467.
Am J Med Genet. 1993 Feb 1;45(3):313-9. doi: 10.1002/ajmg.1320450307.
A series of earlier reports has described the velo-cardio-facial syndrome (VCFS), a syndrome of multiple anomalies including cleft palate, heart malformations, facial characteristics, and learning disabilities. The patients reported previously were primarily ascertained from a craniofacial program at a large tertiary medical center. Recent reports, including a companion paper in this issue, suggest that this common syndrome of clefting is also a common syndrome of congenital heart defect (CHD) which is expressed as familial examples of DiGeorge sequence. Appreciation of more severely affected cases of VCFS and the detection of mild expressions have led to a broadening of the phenotypic spectrum of the syndrome. The purpose of this report is to describe the full spectrum of VCFS, including several new manifestations and to compare the VCFS phenotype with published cases of "familial DiGeorge sequence" which are now thought to represent examples of VCFS.
一系列早期报告描述了腭心面综合征(VCFS),这是一种具有多种异常表现的综合征,包括腭裂、心脏畸形、面部特征以及学习障碍。先前报道的患者主要来自一家大型三级医疗中心的颅面项目。近期的报告,包括本期的一篇相关论文,表明这种常见的腭裂综合征也是一种常见的先天性心脏缺陷(CHD)综合征,表现为DiGeorge序列的家族性病例。对VCFS更严重受累病例的认识以及对轻度表现的发现,导致了该综合征表型谱的拓宽。本报告的目的是描述VCFS的全貌,包括几种新的表现,并将VCFS的表型与现已被认为是VCFS病例的已发表“家族性DiGeorge序列”病例进行比较。