Fodor Lucian, Baruch-Gershoni Ruth, Ullmann Yehuda
Department of Plastic and Reconstructive Surgery Institute of Human Genetics, Rambam Medical Center, The Faculty of Medicine, Technion-Israel Institute of Technology, Haifa Israel.
Clin Dysmorphol. 2006 Jul;15(3):161-163. doi: 10.1097/01.mcd.0000220606.32531.52.
We report a child with multiple anomalies that was born to healthy nonconsanguineous parents after an unremarkable pregnancy. The female infant had bilateral cleft lip and palate, bilateral toe syndactyly (second and third with no bony fusion), multiple bilateral periorbital tumors, ectropion, lagophthalmos, strabismus and prominent eyes. High frontal hairline and everted lower lip were also noted. Soon after delivery, she was referred to the 'Cleft Clinic' where she underwent cleft lip and palate repair. Seven dermoid cysts were also removed from both periorbital areas. Follow-up documented moderate developmental retardation, hypothyroidism and hydronephrosis. Although some features of our patient overlap with those described in ectrodactyly, ectodermal dysplasia and cleft lip/palate, Martinez, Zlotogora-Ogur, Filippi, Freihofer and Blepharocheilodontic syndromes, our patient has a combination of features not previously reported.
我们报告了一名患有多种异常的儿童,其父母健康且非近亲结婚,孕期无异常。该女婴患有双侧唇腭裂、双侧并趾畸形(第二和第三趾,无骨质融合)、双侧眶周多发肿瘤、睑外翻、兔眼症、斜视和突眼。还注意到高额头发际线和下唇外翻。出生后不久,她被转诊至“腭裂诊所”,在那里接受了唇腭裂修复手术。双侧眶周区域还切除了7个皮样囊肿。随访记录显示有中度发育迟缓、甲状腺功能减退和肾积水。尽管我们患者的一些特征与裂手裂足畸形、外胚层发育不良和唇裂/腭裂、马丁内斯综合征、兹洛托戈拉 - 奥古尔综合征、菲利皮综合征、弗赖霍费尔综合征和睑裂唇腭裂综合征中所描述的特征有重叠,但我们的患者具有以前未报告过的特征组合。