首页> 外文期刊>Journal of Cardiovascular Disease Research >A patient with Marfan’s syndrome presented with severe rheumatic mitral stenosis and successfully treated with percutaneous transmitral balloon commissurotomy e Report of first case
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A patient with Marfan’s syndrome presented with severe rheumatic mitral stenosis and successfully treated with percutaneous transmitral balloon commissurotomy e Report of first case

机译:患有马凡氏综合征的患者出现严重的风湿性二尖瓣狭窄,并经皮经皮穿刺球囊合影术成功治疗。

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Marfan’s syndrome (MFS) is an inherited autosomal dominant disorder of connective tissue with mutation on the fibrillin-1 gene encoding for fibrillin. This frequently involves the cardiovascular system with prevalence is 1:5000-10,000. The clinical major criteria involve the skeletal and ocular apparatus and the cardiovascular and central nervous system. In Marfan’s syndrome mitral valve prolapse and aortic dilation are the main cardiovascular manifestations. According to the literature database the prevalence of aortic dilatation is 76%, 62% for mitral valve prolapse, 29% for mitral valve regurgitation and 26% for aortic regurgitation, in adult patients with Marfan’s syndrome. We are reporting a case who presented with severe rheumatic mitral stenosis & later on examination found to be a case of Marfan’s syndrome. This patient was successfully treated with percutaneous transmitral balloon commissurotomy. In medline search, so far there is no other case of Marfan’s syndrome reported to have rheumatic mitral stenosis.
机译:马凡氏综合症(MFS)是结缔组织的遗传性常染色体显性遗传疾病,其纤丝蛋白1编码纤丝蛋白的基因发生突变。这经常涉及心血管系统,患病率为1:5000-10,000。临床主要标准涉及骨骼和眼部设备以及心血管和中枢神经系统。在马凡氏综合征中,二尖瓣脱垂和主动脉扩张是心血管的主要表现。根据文献数据库,在患有Marfan综合征的成年患者中,主动脉扩张的患病率为76%,二尖瓣脱垂的患病率为62%,二尖瓣反流的患病率为29%,二尖瓣反流的患病率为26%。我们正在报告一例患有严重风湿性二尖瓣狭窄的患者,后来经检查发现是马凡氏综合症。该患者经皮经皮球囊吻合术成功治疗。在medline搜索中,到目前为止,尚无其他报道称Marfan综合征患有风湿性二尖瓣狭窄的病例。

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