Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome.
case_report · Level V
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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.
Medical subject headings
- Acrocephalosyndactylia
- Ultrasonography, Prenatal