Philcox D V, Sellars S L, Pamplett R, Beighton P
Brain. 1975 Jun;98(2):309-16. doi: 10.1093/brain/98.2.309.
A kindred with a unique autosomal dominantly inherited ataxia of late onset is described. Manifestations of the condition include defective optokinetic nystagmus and absent or abnormal oculo-vestibular responses, in association with normal cochlear function. It is possible that these latter features may serve as "markers" to indicate the presence of the disease in presymptomatic young adults, thereby facilitating important genetic counseling.
本文描述了一个具有独特的常染色体显性遗传迟发性共济失调的家族。该病症的表现包括视动性眼球震颤缺陷以及眼前庭反应缺失或异常,同时伴有正常的耳蜗功能。这些后者的特征有可能作为“标志物”,用以指示无症状的年轻成年人中疾病的存在,从而便于进行重要的遗传咨询。