Ell J, Prasher D, Rudge P
J Neurol Neurosurg Psychiatry. 1984 Jan;47(1):26-32. doi: 10.1136/jnnp.47.1.26.
Ten patients with an accepted diagnosis of Friedreich's ataxia have been examined neuro-otologically, and oculomotor, vestibular and auditory function assessed. Brainstem auditory evoked potentials (BAEPs) were also recorded. A high incidence of various eye movement disorders was noted. Some of these were indicative of cerebellar dysfunction. Reduced vestibular function and impaired hearing were common to most of the patients. BAEPs were also abnormal in the majority; reasons underlying these abnormalities are discussed. Neuro-otologically, the patients did not constitute an homogeneous group. The findings cast doubt upon the accuracy and validity of the currently accepted criteria for the diagnosis and classification of the spinocerebellar degenerations.
对十名已确诊为弗里德赖希共济失调的患者进行了神经耳科学检查,并评估了其动眼、前庭和听觉功能。还记录了脑干听觉诱发电位(BAEP)。发现各种眼动障碍的发生率很高。其中一些表明存在小脑功能障碍。大多数患者都有前庭功能减退和听力受损的情况。大多数患者的BAEP也异常;讨论了这些异常背后的原因。从神经耳科学角度来看,这些患者并非一个同质群体。这些发现对目前公认的脊髓小脑变性诊断和分类标准的准确性和有效性提出了质疑。