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...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.展开更多
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.
