VELO-CARDIO-FACIAL SYNDROME - A REVIEW OF 120 PATIENTS

被引:340
作者
GOLDBERG, R
MOTZKIN, B
MARION, R
SCAMBLER, PJ
SHPRINTZEN, RJ
机构
[1] MONTEFIORE MED CTR,DEPT PLAST SURG,BRONX,NY 10467
[2] MONTEFIORE MED CTR,CTR CONGENITAL DISORDERS,BRONX,NY 10467
[3] MONTEFIORE MED CTR,DEPT PEDIAT,BRONX,NY 10467
[4] YESHIVA UNIV ALBERT EINSTEIN COLL MED,BRONX,NY 10461
[5] BLYTHEDALE CHILDRENS HOSP,VALHALLA,NY
[6] ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,LONDON,ENGLAND
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 45卷 / 03期
关键词
VELO-CARDIO-FACIAL SYNDROME; DIGEORGE SEQUENCE; CONOTRUNCAL ANOMALY FACE SYNDROME; CARDIAC DEFECT; CLEFT PALATE; MONOSOMY; 22Q11; CONGENITAL HEART ANOMALIES; PSYCHIATRIC DISORDERS;
D O I
10.1002/ajmg.1320450307
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
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.
引用
收藏
页码:313 / 319
页数:7
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