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先天性无舌症与内脏反位。

Congenital aglossia and situs inversus.

作者信息

Dunham M E, Austin T L

机构信息

Department of Surgery, University of South Carolina School of Medicine, Columbia 29203.

出版信息

Int J Pediatr Otorhinolaryngol. 1990 Jun;19(2):163-8. doi: 10.1016/0165-5876(90)90222-d.

Abstract

Lingual agenesis is a rare anomaly caused by failed embryogenesis of the lateral lingual swellings during the fourth and fifth gestational weeks. Most reported cases have been part of oromandibular limb hypogenesis syndromes. A review of the literature reveals two previously reported cases of congenital aglossia and situs inversus. A case of lingual agenesis associated with micrognathia and situs inversus is reported in a newborn presenting with upper airway obstruction at birth.

摘要

舌发育不全是一种罕见的异常情况,由妊娠第4至5周侧舌隆突胚胎发育失败引起。大多数报告病例是口下颌肢体发育不全综合征的一部分。文献回顾显示,此前有两例先天性无舌症合并内脏反位的报道。本文报告了一例舌发育不全合并小颌畸形和内脏反位的病例,该新生儿出生时即出现上呼吸道梗阻。

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