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Ⅱ型遗传性出血性毛细血管扩张症的发病机理研究进展 被引量:4

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摘要 遗传性出血性毛细血管扩张征(hereditary hemorrhagictelangiectasia,HHT),又名Rendu-Osler-Weber综合征,是一种以血管发育异常为特征的常染色体显性遗传病。目前流行病学调查研究显示,该病发病率远比以前认为的要高,在法国约为1/2 351,丹麦的Funen约为1/3 500,美国佛蒙特约为1/6 500,北爱尔兰约为1/39 000。然而,国内尚未有大规模的资料统计。本病的发病与年龄相关,一般在40~45岁左右。
作者 张磊
出处 《血栓与止血学》 2002年第3期131-134,共4页 Chinese Journal of Thrombosis and Hemostasis
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