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。
It is reported that the case of SCA2 with Parkinsonism pedigree which is sensitive to the Levo-dopa treatment is very rare,.
目的报道一个五代母系遗传的未知神经变性疾病家系。
Objective To report a five-generation Chinese family with unidentified maternally transmitted hereditary neurodegenerative disease.
报道了一个遗传性小眼症家系的调查结果，该家系属于先天性睑裂狭小综合症，为常染色体显性遗传。
An investigation of a genetic Blepharostenosis family was reported. It was proved that the disease was congenital eyelid syndrome and autosomal dominant inheritance.
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