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
点击下载:
PDF
(2760KB)
返 回