Shprintzen Robert J
Department of Otolaryngology and Communication Science, Velo-Cardio-Facial Syndrome International Center, State University of New York, Upstate Medical University, Syracuse, NY 13210, USA.
Dev Disabil Res Rev. 2008;14(1):3-10. doi: 10.1002/ddrr.2.
Velo-cardio-facial syndrome is one of the names that has been attached to one of the most common multiple anomaly syndromes in humans. The labels DiGeorge sequence, 22q11 deletion syndrome, conotruncal anomalies face syndrome, CATCH 22, and Sedlacková syndrome have all been attached to the same disorder. Velo-cardio-facial syndrome has an expansive phenotype with more than 180 clinical features described that involve essentially every organ and system. The syndrome has drawn considerable attention because a number of common psychiatric illnesses are phenotypic features including attention deficit disorder, schizophrenia, and bipolar disorder. The expression is highly variable with some individuals being essentially normal at the mildest end of the spectrum, and the most severe cases having life-threatening and life-impairing problems. The syndrome is caused by a microdeletion from chromosome 22 at the q11.2 band. Although the large majority of affected individuals have identical 3 megabase deletions, less than 10% of cases have smaller deletions of 1.5 or 2.0 megabases. The 3 megabase deletion encompasses a region containing 40 genes. The syndrome has a population prevalence of approximately 1:2,000 in the United States, although incidence is higher. Although initially a clinical diagnosis, today velo-cardio-facial syndrome can be diagnosed with extremely high accuracy by fluorescence in situ hybridization and several other laboratory techniques. Clinical management is age dependent with acute medical problems such as congenital heart disease, immune disorders, feeding problems, cleft palate, and developmental disorders occupying management in infancy and preschool years. Management shifts to cognitive, behavioral, and learning disorders during school years, and then to the potential for psychiatric disorders including psychosis in late adolescence and adult years. Although the majority of people with velo-cardio-facial syndrome do not develop psychosis, the risk for severe psychiatric illness is 25 times higher for people affected with velo-cardio-facial syndrome than that of the general population. Therefore, interest in understanding the nature of psychiatric illness in the syndrome remains strong.
心脏-颜面综合征是人类最常见的多重异常综合征之一的名称。迪乔治序列、22q11缺失综合征、圆锥动脉干异常颜面综合征、CATCH 22和塞德拉克娃综合征等名称都被用于指代同一种疾病。心脏-颜面综合征具有广泛的表型,已描述的临床特征超过180种,几乎涉及每个器官和系统。该综合征引起了相当大的关注,因为一些常见的精神疾病是其表型特征,包括注意力缺陷障碍、精神分裂症和双相情感障碍。其表现高度可变,在症状最轻的一端,一些个体基本正常,而最严重的病例则有危及生命和影响生活的问题。该综合征是由22号染色体q11.2带的微缺失引起的。虽然绝大多数受影响个体有相同的3兆碱基缺失,但不到10%的病例有1.5或2.0兆碱基的较小缺失。3兆碱基的缺失包含一个含有40个基因的区域。在美国,该综合征的人群患病率约为1:2000,尽管发病率更高。虽然最初是临床诊断,但如今通过荧光原位杂交和其他几种实验室技术可以极其准确地诊断心脏-颜面综合征。临床管理取决于年龄,先天性心脏病、免疫紊乱、喂养问题、腭裂和发育障碍等急性医疗问题在婴儿期和学龄前阶段占据管理重点。在学龄期,管理重点转向认知、行为和学习障碍,然后在青少年晚期和成年期转向包括精神病在内的精神疾病的可能性。虽然大多数心脏-颜面综合征患者不会发展为精神病,但心脏-颜面综合征患者患严重精神疾病的风险比普通人群高25倍。因此,人们对了解该综合征中精神疾病的本质仍兴趣浓厚。