1) spinocerebellar ataxia type2
脊髓小脑共济失调2型
1.
Clinical characteristics and MRI features of 8 spinocerebellar ataxia type2 and type3 patients;
8例脊髓小脑共济失调2型、3型患者的临床表型及MRI表现分析
2) spinocerebellar ataxia type 1
脊髓小脑共济失调1型
1.
Clinical analysis on the cases with intermediate Cytosine-Adenine-Guanine repeat alleles of spinocerebellar ataxia type 1;
脊髓小脑共济失调1型中等重复动态突变患者临床表型分析
3) spinocerebellar ataxia
脊髓小脑型共济失调
1.
Clinical characteristics and genetic diagnosis of hereditary spinocerebellar ataxia type 7;
遗传性脊髓小脑型共济失调7型遗传学诊断及临床特征
4) Spinocercbellar ataxia type 3
脊髓小脑共济失调3型
1.
Objective: To detect the clinical features of patients of Spinocercbellar ataxia type 3 (SCA3/MJD),we knowed its clinical characteristics detailedly.
目的:通过对新疆脊髓小脑共济失调3型(SCA3/MJD)家系患者的临床表现的调查,了解其临床特点,并对家系成员及患者进行基因分析,进而研究该疾病临床表现与基因突变的关系,同时作出基因诊断和症状前诊断。
5) SCA2 with Parkinsonism
帕金森氏病特征的脊髓小脑共济性失调2型
补充资料：脊髓遗传型共济失调
脊髓遗传型共济失调
即"脊髓型共济失调"。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条