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对散发性运动神经元病患者进行肯尼迪病筛查的阳性率较低。

Low yield in screening patients with sporadic motor neuron disease for Kennedy disease.

作者信息

Saunderson R B, Yu B, Trent R J A, Pamphlett R

机构信息

Department of Pathology (The Stacey MND Laboratory), The University of Sydney, Sydney, New South Wales, Australia.

出版信息

Intern Med J. 2007 Nov;37(11):772-4. doi: 10.1111/j.1445-5994.2007.01499.x.

Abstract

The diagnostic yield of testing for Kennedy disease in patients diagnosed with sporadic motor neuron disease (MND) is unclear. We measured the CAG repeat lengths in the androgen receptor gene of patients with progressive limb weakness who had either upper and lower motor signs (n = 130), or lower motor neuron signs alone (n = 30). Only one patient with a long history of lower motor weakness had a repeat length in the Kennedy disease range. Testing for Kennedy disease is unlikely to benefit MND patients with upper motor neuron signs or those with a short history of lower motor signs.

摘要

对于诊断为散发性运动神经元病(MND)的患者,检测肯尼迪病的诊断率尚不清楚。我们测量了患有进行性肢体无力且有上、下运动神经元体征(n = 130)或仅有下运动神经元体征(n = 30)患者的雄激素受体基因中的CAG重复序列长度。只有一名有长期下运动神经元无力病史的患者其重复序列长度在肯尼迪病范围内。对有上运动神经元体征的MND患者或下运动神经元体征病史较短的患者进行肯尼迪病检测不太可能有益。

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