[III型遗传性运动和感觉神经病。病例报告及文献综述]
[Hereditary motor and sensory neuropathy type III. Case report and review of the literature].
作者信息
Haverkamp F, Behring B
机构信息
Zentrum für Kinderheilkunde, Universität Bonn.
出版信息
Klin Padiatr. 1995 Jan-Feb;207(1):24-7. doi: 10.1055/s-2008-1046504.
PMID:7885014
Abstract
We report on a 6 years old girl, who was first presented at the age of 3 1/2 years with progressive ataxia, coordination disturbance and distal motoric weakness (especially hand-weakness). Diagnostic procedure revealed heredomotorsensoric neuropathy type III (syn. Dejerine-Sottas Disease).
摘要
我们报告了一名6岁女孩，她在3岁半时首次出现进行性共济失调、协调障碍和远端运动无力（尤其是手部无力）。诊断程序显示为III型遗传性运动感觉神经病（又称Dejerine-Sottas病）。
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