A rare cause of intracranial hemorrhage:: Factor X deficiency

被引：13

作者：

Çitak, A ^{[1
]}

Üçsel, R ^{[1
]}

Karaböcüoglu, M ^{[1
]}

Ünüvar, A ^{[1
]}

Uzel, N ^{[1
]}

机构：

[1] Istanbul Univ, Inst Child Hlth, Dept Pediat Emergency, Istanbul, Turkey

来源：

PEDIATRIC EMERGENCY CARE | 2001年 / 17卷 / 05期

关键词：

Factor X deficiency; intracranial hemorrhage;

D O I：

10.1097/00006565-200110000-00007

中图分类号：

R4 [临床医学];

学科分类号：

1002 ; 100602 ;

摘要：

Congenital factor X deficiency is a rare inherited coagulation disorder, characterized by prolonged prothrombin time and partial thromboplastin time. For the definite diagnosis, specific factor X level should be investigated. We describe a patient with factor X deficiency who had intracranial hemorrhage. Hematologic tests showed prolonged prothrombin time, partial thromboplastin time, and a factor X level of 5%. The patient's hemorrhage resolved with fresh frozen plasma replacement. In this article, we discuss the clinical features and management of factor X deficiency.

引用

页码：349 / 350

页数：2

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