Di Maio L, Marcelli V, Vitale C, Menzione M, De Giorgio A, Briganti F, Perretti A, Marciano E, Filla A, De Michele G
Dipartimento di Scienze Neurologiche, Università Federico II Naples, Italy.
Can J Neurol Sci. 2006 May;33(2):237-9. doi: 10.1017/s0317167100005059.
The cervico-oculo-acoustic syndrome comprises Klippel-Feil anomaly, sensorineural deafness and Duane's retraction syndrome. Polygenic, autosomal dominant, and X-linked inheritance have been hypothesized. The disorder has rarely been reported in males.
A 42-year-old male, born of consanguineous parents, presented with Duane's syndrome, mixed hearing loss, C2-C3 fusion, neck stiffness, and right facial palsy. A variety of cardiac, neurological and urogenital anomalies occurred in his relatives. The electro-oculographic studies showed impaired abduction and adduction of the right eye and impaired abduction of the left eye. Vergence, vertical eye movements and peripheral vestibular responses were normal. Somatosensory evoked potentials showed absence of the N13 peak and brainstem auditory evoked potentials bilateral delay of the I-III interpeak latencies.
Consanguinity of the patient's parents, not previously reported, suggests autosomal recessive inheritance, but autosomal dominant inheritance is indicated by the family history. The pattern of the oculomotor deficit is consistent with bilateral dysplasia of the abducens nuclei with preserved internuclear neurons in the right abducens nucleus. Neurophysiological investigations revealed lower brainstem and cervical cord involvement.
颈眼耳综合征包括克利佩尔-费尔综合征、感音神经性耳聋和杜安眼球后退综合征。曾有关于多基因、常染色体显性和X连锁遗传的假说。该疾病在男性中鲜有报道。
一名42岁男性,父母近亲结婚,患有杜安综合征、混合性听力损失、C2 - C3融合、颈部僵硬和右侧面瘫。其亲属中出现了多种心脏、神经和泌尿生殖系统异常。眼电图研究显示右眼外展和内收受损,左眼外展受损。辐辏、垂直眼球运动和外周前庭反应正常。体感诱发电位显示N13波峰缺失,脑干听觉诱发电位双侧I - III峰间潜伏期延迟。
患者父母近亲结婚,此前未见报道,提示常染色体隐性遗传,但家族史提示常染色体显性遗传。眼球运动缺陷模式与展神经核双侧发育异常一致,右侧展神经核中的核间神经元保留。神经生理学研究显示脑桥下部和颈髓受累。