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两个家族中的毛细血管扩张症和血管性血友病

Telangiectasia and von Willebrand's disease in two families.

作者信息

Conlon C L, Weinger R S, Cimo P L, Moake J L, Olson J D

出版信息

Ann Intern Med. 1978 Dec;89(6):921-4. doi: 10.7326/0003-4819-89-6-921.

Abstract

Two families are described with members who have both von Willebrand's disease and telangiectasias. Family A has four members in three consecutive generations that have both von Willebrand's disease and telangiectasias. von Willebrand's disease in this family is characterized by decreased ristocetin cofactor (FVIII-vWF), variably depressed factor VIII coagulant (FVIII-AHG), and factor VIII-related antigen (FVIII-AGN) levels. FVIII-AGN mobility on two-dimensional crossed immunoelectrophoresis was found to be normal. Four generations in Family B have von Willebrand's disease characterized by decreased FVIIII-AHG, FVIII-vWF, FVIII-AGN, and prolonged template bleeding times. Two members of this family also have telangiectasias and recurrent gastrointestinal bleeding. Results in these two families suggest an association between von Willebrand's disease and telangiectasia--perhaps a defect in vascular endothelial cell function.

摘要

本文描述了两个家族,其成员同时患有血管性血友病和毛细血管扩张症。家族A连续三代中有四名成员同时患有血管性血友病和毛细血管扩张症。该家族的血管性血友病特征为瑞斯托菌素辅因子(FVIII-vWF)降低、凝血因子VIII促凝活性(FVIII-AHG)不同程度降低以及因子VIII相关抗原(FVIII-AGN)水平降低。二维交叉免疫电泳显示FVIII-AGN迁移率正常。家族B的四代成员患有血管性血友病,其特征为FVIII-AHG、FVIII-vWF、FVIII-AGN降低以及模板出血时间延长。该家族的两名成员还患有毛细血管扩张症和复发性胃肠道出血。这两个家族的结果提示血管性血友病与毛细血管扩张症之间存在关联——可能是血管内皮细胞功能缺陷。

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