SCA2 with Parkinsonism 帕金森氏病特征的脊髓小脑共济性失调2型
It is reported that the case of SCA2 with Parkinsonism pedigree which is sensitive to the Levo-dopa treatment is very rare,.
国外文献报道，在欧美人群中，这种呈帕金森氏综合症的对多巴胺治疗敏感的SCA2家系很少。
Methods The length of genetic segment of SCA1, SCA2 and SCA3 in 92 patients with ataxia of unknown origin were detected by polymerase chain reaction (PCR) and agarose gel electrophoresis.
方法应用PCR方法和琼脂糖凝胶电泳对92例不明原因共济失调先证患者测定其SCA1、SCA2和SCA3基因片段长度。
Conclusion the incidence of SCA1, SCA2 and SCA3 is 22.8% in patients with ataxia of unknown origin, and SCA3 is main type. Genetic analysis is the most effective means for the diagnosis of SCA.
结论通过这次研究，发现SCA1、SCA2、SCA3型在不明原因的共济失调中的发生率为22.8%，其中又以SCA3型为主，确定诊断的最直接最有效的手段是基因诊断。
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