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Congenital Hypofibrinogenemia: A Distinct Entity? Report Of Three Cases In The Same Family

 

作者: CapelP.,   DedrieJ.,   DetrainC.,   RauisM.,   FonduP.,  

 

期刊: Acta Clinica Belgica  (Taylor Available online 1987)
卷期: Volume 42, issue 5  

页码: 342-346

 

ISSN:1784-3286

 

年代: 1987

 

DOI:10.1080/22953337.1987.11719246

 

出版商: Taylor&Francis

 

数据来源: Taylor

 

摘要:

SummaryThree patients in the same family with low fibrinogen levels have been studied. The abnormality was clinically silent. The fibrinogen level varied from 50 to 145 mg/dl. Good agreement between the various methods of fibrinogen assay was observed. Since no afibrinogenemic patient was observed in this family, the abnormality presented by these patients was classified as congenital hypofibrinogenemia. Our observation also suggests that there is an increase in fibrinogen level with age in hypofibrinogcnemic patients, as occurs in normal subjects.

 

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