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Prenatal diagnosis and management of Apert syndrome in a low-middle income country: Case report

9 Aug 2024

Abstract excerpt

INTRODUCTION AND IMPORTANCE: Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, midface hypoplasia, and syndactyly. Prenatal diagnosis of this condition can be challenging. This case report highlights the importance of recognizing characteristic ultrasound findings for timely diagnosis and genetic counselling. CASE PRESENTATION: A 37-year-old, gravida 1, para 0 woman underwent...

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PMID: 39128215
DOI: 10.1016/j.ijscr.2024.110134

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