Nager Syndrome: A Case Report

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• 作者：Ju-Li Lin ; ^{lin001@cgmh.org.tw}
• 关键词：micrognathia ; Nager syndrome ; preaxial acrofacial dysostosis ; tracheostomy
• 刊名：Pediatrics Neonatology
• 出版年：2012
• 出版时间：April, 2012
• 年：2012
• 卷：53
• 期：2
• 页码：147-150
• 全文大小：548 K

文摘

Nager syndrome (preaxial acrofacial dysostosis) is rare and mostly sporadic. We present a case of Nager syndrome in Taiwan. Craniofacial findings included micrognathia, malar hypoplasia, downslanting palpebral fissures, cleft palate, and ear anomalies. Radial defects consisted of hypoplastic thumb, short forearm, and proximal radioulnar synostosis. Patent ductus arteriosus, atrial septal defect, lower limb deformities, and uncommon flat nasal bridge were noted. Nasal endotube passing through a narrowing oropharynx region or oral airway is life-saving before tracheostomy is performed on patients with Nager syndrome and restricted jaw opening and glossoptosis.