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编号:11027494
Fabry病临床报告及病理学研究
http://www.100md.com 《临床心身疾病杂志》 2005年第4期
Fabry病;血管角质瘤;а半乳糖苷酶,,Fabry病;血管角质瘤;а半乳糖苷酶,【摘要】,【关键词】,1临床资料,2病理改变,3讨论,参考文献
     【摘要】 目的 探讨Fabry病的临床特点及其病理学特征。 方法 通过1例Fabry病患者详细的临床资料,检索国内外相关资料,研究Fabry病的发病机制、临床特征、治疗及预后。 结果 典型的临床表现结合特征性病理改变可诊断Fabry病。 结论 Fabry病为罕见的代谢性遗传性疾病,加强对该病的认识,减少误诊,加强产前诊断可降低本病的发生率。

     【关键词】 Fabry病;血管角质瘤;а半乳糖苷酶

    Clinical report and pathological study of Fabry disease

    Li Xiaoyan, Xie Huijun, Zhang Xian, et al

    (Ruici hospital of Nantong , 226010,Jiangsu, China)

    【Abstract】 Objective To investigative clinical and pathological features of Fabry disease. Methods According to detailed clinical data of a patient with Fabry disease and related data in home and abroad, authors studied the pathogenic mechanism, clinical feature, therapy and prognosis of the disease. Results Diagnosis of Fabry disease might be depended on typical clinical manifestations and characteristic pathological changes. Conclusion Fabry disease is a uncommon metabolic genetic disease. The misdiagnosis can reduce if reinforcing the cognizance of the Fabry disease, and the incidence rate will reduce by fortifying prenatal diagnosis. ......

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