Higashi K, Edo M
Department of Otolaryngology, Akita University, Japan.
J Laryngol Otol. 1996 Nov;110(11):1057-9. doi: 10.1017/s0022215100135741.
Aglossia is a rare anomaly often accompanied with several congenital defects including varying degrees of limb deficiency, micrognathia and oral synechiae. We report on a girl with aglossia and persistent anterior buccopharyngeal membrane. Other anomalies observed on the patient were oesophageal atresia, hypoplastic epiglottis, ptosis of the left eyelid, and conductive deafness which is probably an additional symptom of this syndrome group.
无舌畸形是一种罕见的异常情况,常伴有多种先天性缺陷,包括不同程度的肢体缺损、小颌畸形和口腔粘连。我们报告了一名患有无舌畸形和持续性颊咽前膜的女孩。在该患者身上观察到的其他异常情况包括食管闭锁、会厌发育不全、左眼睑下垂以及传导性耳聋,后者可能是该综合征组的另一个症状。