Dispute diagnosis of Friedreich's ataxia.

M. Nuwer
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Abstract

To the Editor .—I would like to question respectfully the article entitled "Auditory Function in Friedreich's Ataxia: Electrophysiologic Study of a Family" by Shanon et al published in the AprilArchives(1981;107:254-256). First, the inherited ataxias are a large, diverse, heterogeneous group of disorders. 1 Friedreich's ataxia forms a subgroup with rather specific symptoms. 2 Scientifically, it is important to separate patients with Friedreich's ataxia from others with inherited ataxias. However, Shanon et al do not describe in this family the typical scoliosis, cardiomyopathy, diabetes, corticospinal tract dysfunction, and other characteristics. Without the usual recessive inheritance pattern, these other features are important for making a diagnosis. As suggested by Barbeau, 2 the eponym "Friedreich's" should be avoided in atypical families. The second difficulty I have is with the latencies of their auditory brainstem potentials (ABPs). On close inspection, the latencies seem to be within generally accepted normal limits 3 in
弗里德赖希共济失调的诊断争议。
致编辑:我想恭敬地质疑香农等人在四月档案(1981;107:254-256)上发表的题为“弗里德赖希共济失调中的听觉功能:一个家庭的电生理研究”的文章。首先,遗传性共济失调是一个庞大的、多样的、异质性的疾病群体。弗里德赖希共济失调症是一个亚组,其症状相当特殊。从科学上讲,将弗里德里希共济失调患者与其他遗传性共济失调患者区分开来是很重要的。然而,Shanon等人没有描述该家族典型的脊柱侧凸、心肌病、糖尿病、皮质脊髓束功能障碍等特征。没有通常的隐性遗传模式,这些其他特征对诊断很重要。正如Barbeau所建议的那样,在非典型家庭中应该避免使用“弗里德赖希”这个名字。我遇到的第二个困难是他们的听觉脑干电位(ABPs)的潜伏期。仔细检查,延迟似乎在一般接受的正常范围3英寸
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