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.
点击下载:
PDF (3572KB)
返 回