Walker S J, Ball R H, Babcook C J, Feldkamp M M
Department of Radiology, University of Utah Health Sciences Center, Salt Lake City 84132, USA.
J Ultrasound Med. 2001 Nov;20(11):1175-80; quiz 1181-2. doi: 10.7863/jum.2001.20.11.1175.
To determine the prevalence of aneuploidy and additional major anatomic abnormalities in fetuses and neonates with cleft lip with or without cleft palate.
All cases of cleft lip with or without cleft palate (cleft lip/cleft palate) occurring in Utah from 1995 through 1999 were reviewed by using the Utah Birth Defect Network population-based surveillance system. All pregnancy outcomes are included (stillborn, live born, and termination) in this analysis.
Of 263 cases of cleft lip/cleft palate, 72 (27.4%) were unilateral cleft lip, 112 (42.6%) were unilateral cleft lip and cleft palate, 12 (4.6%) were bilateral cleft lip, and 67 (25.5%) were bilateral cleft lip and cleft palate. Fifteen (5.7%) of the 263 fetuses and neonates were aneuploid. One (1.2%) with cleft lip (unilateral and bilateral combined) was aneuploid. Five (4.5%) of the fetuses and neonates with unilateral cleft lip and cleft palate were aneuploid compared with 9 (13.4%) of fetuses and neonates with bilateral cleft lip and cleft palate. In known or presumed euploid fetuses and neonates, additional sonographically occult major anatomic abnormalities occurred in 5 (7.0%) of 71 with unilateral cleft lip, 18 (16.8%) of 107 with unilateral cleft lip and cleft palate, 1 (8.3%) of 12 with bilateral cleft lip, and 12 (20.7%) of 58 with bilateral cleft lip and cleft palate. These abnormalities primarily involved the heart and the central nervous system.
Amniocentesis for karyotype should be offered in all cases of cleft lip/cleft palate because of the risk of aneuploidy. Patients should be counseled that sonographically occult additional anatomic abnormalities might be present with all clefts.
确定伴有或不伴有腭裂的唇裂胎儿及新生儿中非整倍体及其他主要解剖学异常的患病率。
利用基于犹他州出生缺陷网络人群的监测系统,对1995年至1999年在犹他州发生的所有伴有或不伴有腭裂的唇裂(唇裂/腭裂)病例进行回顾。本分析纳入了所有妊娠结局(死产、活产和终止妊娠)。
在263例唇裂/腭裂病例中,72例(27.4%)为单侧唇裂,112例(42.6%)为单侧唇裂合并腭裂,12例(4.6%)为双侧唇裂,67例(25.5%)为双侧唇裂合并腭裂。263例胎儿及新生儿中15例(5.7%)为非整倍体。1例(1.2%)唇裂(单侧和双侧合并)为非整倍体。单侧唇裂合并腭裂的胎儿及新生儿中有5例(4.5%)为非整倍体,而双侧唇裂合并腭裂的胎儿及新生儿中有9例(13.4%)为非整倍体。在已知或推测为整倍体的胎儿及新生儿中,71例单侧唇裂中有5例(7.0%)、107例单侧唇裂合并腭裂中有18例(16.8%)、12例双侧唇裂中有1例(8.3%)、58例双侧唇裂合并腭裂中有12例(20.7%)存在超声检查隐匿的其他主要解剖学异常。这些异常主要累及心脏和中枢神经系统。
由于存在非整倍体风险,所有唇裂/腭裂病例均应进行羊水染色体核型分析。应告知患者,所有唇裂都可能存在超声检查隐匿的其他解剖学异常。