| 2 | 应用三维最大模式产前诊断Apert综合征显示文摘Apert syndrome is a rare disorder characterized by coronal craniosynostosis, syndactyly, brachycephaly, midfacial hypoplasia, and central nervous system anomalies, among other malformations. We present a case of Apert syndrome examined at 22 +0 weeks’gestation. Three-dimension-almaximum mode was decisive for the correct prenatal diagnosis by demonstrating the cranial deformities. | Esser T. Rogalla P. Bamberg C. Kalache K.D. 高雪莲 | 2006 | 世界核心医学期刊文摘(妇产科学分册)2006，0，3： | 0 |
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