| Literature DB >> 16260220 |
Tilman Esser1, Patrick Rogalla, Christian Bamberg, Karim D Kalache.
Abstract
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-dimensional maximum mode was decisive for the correct prenatal diagnosis by demonstrating the cranial deformities.Entities:
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Year: 2005 PMID: 16260220 DOI: 10.1016/j.ajog.2005.07.043
Source DB: PubMed Journal: Am J Obstet Gynecol ISSN: 0002-9378 Impact factor: 8.661