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A Hereditary Dysfibrinogenemia: Fibrinogen Awaji

 

作者: T. Matsuo,   S. Okuno,   T. Mukaida,   S. Ueshima,   K. Okada,   O. Matsuo,  

 

期刊: Pathophysiology of Haemostasis and Thrombosis  (Karger Available online 1987)
卷期: Volume 17, issue 1-2  

页码: 89-97

 

ISSN:1424-8832

 

年代: 1987

 

DOI:10.1159/000215563

 

出版商: S. Karger AG

 

关键词: Fibrinogen;Dysfibrinogenemia

 

数据来源: Karger

 

摘要:

Abnormal function of fibrinogen was observed in a 2 5-year-old woman with no symptoms attributable to dysfibrinogenemia. Disturbed polymerization of fibrin monomer was identified, but the release of fibrinopeptide from the purified fibrinogen and the cross-linking by factor XIII were normal. Other abnormal findings included a high value of fibrinogen degradation products, rapid mobility on immunoelectrophoresis and abnormal spot of γ-chain on two-dimensional polyacrylamide gel electrophoresis. Similar abnormalities were also observed among the patient’s family membe

 

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