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脑腱黄瘤病的临床和疾病基因的表现
Clinical and Pathogenetic Aspects in the Cerebrotendinous Xanthomatosis
【摘要】 脑腱黄瘤病是一种线粒体固醇27羟化酶缺乏的常染色体隐性遗传疾病,临床表现和致病基因表现的有利于临床医生诊断本病。文中就脑腱黄瘤病的临床表现、CYP27A1基因突变、病理和发病机制、治疗方法等研究进行介绍。
【Abstract】 Cerebrotendinous xanthomatosis(CTX) is an autosomal recessive disease due to defective activity of the mitochondrial enzyme sterol 27-hydroxylase. Clinical manifestation, mutation of CYP27 A1 gene, pathogenetic aspects and the treatment of CTX were reviewed.
【关键词】 脑腱黄瘤病;
CYP27A1基因;
临床表现;
【Key words】 cerebrotendinous xanthomatosis; CYP27A1 gene; clinical manifestation;
【Key words】 cerebrotendinous xanthomatosis; CYP27A1 gene; clinical manifestation;
- 【文献出处】 中国临床神经科学 ,Chinese Journal of Clinical Neurosciences , 编辑部邮箱 ,2018年02期
- 【分类号】R741
- 【被引频次】3
- 【下载频次】263