病例报告

以肢体无力为主要表现的原发性家族性脑钙化症一例报告

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  • 1.上海交通大学医学院附属瑞金医院神经内科,上海 200025
    2.江苏省启东市中医院脑病科,江苏 启东 226200

收稿日期: 2019-11-26

  网络出版日期: 2020-02-25

基金资助

上海交通大学医学院高峰高原计划——“研究型医师”(2017);上海市“医苑新星”计划杰出青年医学人才

本文引用格式

周敏慧, 谢心怡, 任汝静, 王刚 . 以肢体无力为主要表现的原发性家族性脑钙化症一例报告[J]. 诊断学理论与实践, 2020 , 19(1) : 92 -94 . DOI: 10.16150/j.1671-2870.2020.01.019

参考文献

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[5] Yao XP, Cheng X, Wang C, et al. Biallelic mutations in MYORG cause autosomal recessive primary familial brain calcification[J]. Neuron, 2018, 98(6):1116-1123.
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[7] Oliveira JR, Oliveira MF. Primary brain calcification in patients undergoing treatment with the biphosphanate alendronate[J]. Sci Rep, 2016, 6:22961.
[8] Hozumi I, Kohmura A, Kimura A, et al. High levels of copper, zinc, iron and magnesium, but not calcium, in the cerebrospinal fluid of patients with fahr's disease[J]. Case Rep Neurol, 2010, 2(2):46-51.
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