HYPERCOAGULABILITY IN A PATIENT WITH MARFAN-SYNDROME

被引：4
|
作者：
HUMPHRIES, JE
STOUFFER, GA
KELLY, TE
ROSE, CE
机构：
[1] UNIV VIRGINIA,SCH MED,DEPT INTERNAL MED,DIV CARDIOL,CHARLOTTESVILLE,VA 22908
[2] UNIV VIRGINIA,SCH MED,DEPT INTERNAL MED,DIV PULM & CRIT CARE MED,CHARLOTTESVILLE,VA 22908
[3] UNIV VIRGINIA,SCH MED,DEPT PEDIAT,CHARLOTTESVILLE,VA 22908
来源：
JOURNAL OF MEDICAL GENETICS | 1991年 / 28卷 / 05期
关键词：
D O I：
10.1136/jmg.28.5.349
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
A 39 year old man with Marfan syndrome presented with multiple pulmonary emboli and renal, hepatic, and splenic infarcts of unknown aetiology. The combination of thromboemboli and physical features initially suggested homocystinuria; however, laboratory examination showed no evidence for this disorder. Laboratory evaluation identified no coagulation abnormalities. This patient represents the unusual occurrence of hypercoagulability in a patient with Marfan syndrome.
引用
收藏
页码：349 / 351
页数：3
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