Izadi Farzad, Ahmadi Aslan, Zobairy Hosna, Bakhti Sepideh, Hirbod Hengameh, Safdarian Mahdi
Department of Otolaryngology, Head and Neck Surgery, Iran University of Medical Sciences, Tehran, Iran.
Department of Otolaryngology, Head and Neck Surgery, Iran University of Medical Sciences, Tehran, Iran.
Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1959-62. doi: 10.1016/j.ijporl.2015.08.043. Epub 2015 Sep 4.
Fraser syndrome is a rare genetic disorder characterized by cryptophthalmos, syndactyly and laryngeal atresia. Although laryngeal webs occur uncommonly, they are the main cause of death in the first week of life in these patients. In this paper, we report two cases of Fraser syndrome with laryngeal webs. One of them was a twelve-year-old girl, primarily diagnosed with a supraglottic laryngeal web. In the course of treatment, a second web was also identified at the level of vocal cords, which is to our knowledge the first case of Fraser syndrome with two laryngeal webs in different levels.
弗雷泽综合征是一种罕见的遗传性疾病，其特征为隐眼畸形、并指（趾）畸形和喉闭锁。虽然喉蹼并不常见，但它们是这些患者出生后第一周死亡的主要原因。在本文中，我们报告了两例伴有喉蹼的弗雷泽综合征病例。其中一例是一名12岁女孩，最初被诊断为声门上喉蹼。在治疗过程中，还在声带水平发现了第二个喉蹼，据我们所知，这是首例不同水平出现两个喉蹼的弗雷泽综合征病例。
Zotero 插件