Hageman G, Ippel P F, Jansen E N, Rozeboom A R
Department of Neurology, Medical Spectrum Twente, Enschede, The Netherlands.
Eur Neurol. 1990;30(6):310-3. doi: 10.1159/000117362.
In this paper we present a study of 6 cases, running through three generations of a Dutch family, with alternating Bell's palsy in an autosomal dominant mode of inheritance. The study included medical history data, neurological examination, blood glucose tests, electromyography, orbicularis oculi reflexes and radiological investigation. In 3 cases a bilateral hypoplasia or scanty cellularization of the mastoid bone and a unilateral obtuse tip of the petrous part of the temporal bones were found. These findings may be a potential inherited etiologic factor.
在本文中，我们展示了一项对一个荷兰家族三代人中6例常染色体显性遗传交替性贝尔麻痹病例的研究。该研究包括病史数据、神经学检查、血糖测试、肌电图、眼轮匝肌反射及放射学检查。在3例病例中发现乳突骨双侧发育不全或细胞形成稀少，以及颞骨岩部单侧钝尖。这些发现可能是一个潜在的遗传病因因素。
