CONSTITUTIONAL HEPARIN CO-FACTOR II DEFICIENCY ASSOCIATED WITH RECURRENT THROMBOSIS

CONSTITUTIONAL HEPARIN CO-FACTOR II DEFICIENCY ASSOCIATED WITH RECURRENT THROMBOSIS
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与复发性血栓形成相关的结构性肝素辅因子 II 缺乏

DOI:
10.1016/s0140-6736(85)92737-0
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发表时间:
1985
期刊:
The Lancet
影响因子:
--
通讯作者:
B. Boneu
B. Boneu
中科院分区:
--
文献类型:
--
作者:
P. Sié;J. Pichon;D. Dupouy;B. Boneu

文献摘要

被引文献

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一名36岁男性复发性深静脉血栓形成和肝素辅助因子II (HC II)缺乏症的家庭被调查这种缺乏症。该缺陷作为常染色体显性性状遗传。4名家族成员HC II水平低,但只有先证者有血栓病史;然而,受影响的4人中有2人只有14岁和23岁。缺乏肝素并不影响患者接受治疗的肝素的抗凝作用。
The family of a 36-year-old man with recurrent deep venous thrombosis and heparin co-factor II (HC II) deficiency was investigated for this deficiency. The deficiency was inherited as an autosomal dominant trait. 4 members of the family had low HC II levels but only the proband had a history of thromboses; however, 2 of 4 affected were only 14 and 23 years old. The deficiency did not affect the anticoagulant action of heparin, with which the patient was treated.