两名患有急性心肌梗死的同胞兄妹存在纯合子因子V莱顿突变：年轻人心肌梗死的罕见病因。
Homozygous factor V Leiden mutation in two siblings presenting with acute myocardial infarction: a rare cause of myocardial infarction in the young.
作者信息
Kaykçoğlu Meral, Hasdemir Can, Eroğlu Zuhal, Kosova Buket, Can Levent H, Ildizli Muge, Yavuzgil Oguz, Payzin Serdar, Turkoglu Cuneyt
机构信息
Department of Cardiology, Ege University, Medical School, 11/2 Bornova Izmir, Turkey.
出版信息
Blood Coagul Fibrinolysis. 2005 Jun;16(4):281-6. doi: 10.1097/01.mbc.0000169221.38797.9c.
Although factor V Leiden mutation, is the most common established genetic risk factor for venous thrombosis, its effect on the development of myocardial infarction remains unclear. We describe a family case of homozygous factor V Leiden mutation in two siblings presenting with acute myocardial infarction as a rare cause of myocardial infarction in the young.
尽管因子V莱顿突变是静脉血栓形成最常见的确立的遗传危险因素，但其对心肌梗死发生发展的影响仍不明确。我们描述了一个家族病例，两名患有急性心肌梗死的兄弟姐妹存在纯合子因子V莱顿突变，这是年轻人心肌梗死的罕见病因。
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