Gacek R R
Ann Otol Rhinol Laryngol. 1976 Jan-Feb;85(1 Pt 1):90-3. doi: 10.1177/000348947608500116.
Familial bilateral abductor cord paralysis was described in the father and two sons of a family in which the ramaining siblings (obe boy and three girls) were normal. The onset of stridor ranged from six months to nine years after birth in these patients who were all treated with a tracheostomy. Normal development and intelligence was experienced by all three patients. Since previous reports of hereditary abductor cord paralysis described mental retardation in all patients who were maintained without tracheostomy, anoxia from unrelieved laryngeal obstruction may be a significant complication following nonsurgical management of patients who appear to tolerate bilateral abductor vocal cord paralysis.
一个家族中,父亲和两个儿子患有家族性双侧声带外展麻痹,其余兄弟姐妹(一个男孩和三个女孩)均正常。这些患者出生后6个月至9岁时出现喘鸣,均接受了气管切开术治疗。三名患者发育和智力均正常。由于先前关于遗传性声带外展麻痹的报告描述了所有未行气管切开术治疗患者均有智力发育迟缓,对于看似能耐受双侧声带外展麻痹的患者,非手术治疗后未缓解的喉梗阻导致的缺氧可能是一个严重并发症。