A Case Report Describing Insights into the Imaging of Apert Syndrome
Rare(2024)
摘要
Apert syndrome is a rare congenital autosomal dominant acrocephalosyndactyly type I syndrome which manifests in the form of various craniofacial, skeletal, and visceral anomalies. The present case reports this rare entity in a 15-month-old who presented with multiple craniofacial abnormalities, craniosynostosis and bilateral symmetrical syndactyly, and after thorough evaluation was diagnosed as a case of Apert Syndrome.
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关键词
Acrocephalosyndactyly,Congenital,Craniosynostosis,Syndactyly,Apert syndrome
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