» Articles » PMID: 2061889

Dysfibrinogenemia Associated with Thrombosis and Third-trimester Fetal Loss. A Case Report

Overview
Journal J Reprod Med
Date 1991 May 1
PMID 2061889
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Dysfibrinogenemias are rare genetic disorders that are clinically silent, cause a mild bleeding tendency or have thromboembolic manifestations. During pregnancy they often cause hemorrhage and first-trimester abortions. A patient with a severe thrombotic tendency during pregnancy had a third-trimester fetal loss.

Citing Articles

Congenital dysfibrinogenemia misdiagnosed and inappropriately treated as acute fatty liver in pregnancy: A case report and review of literature.

Jia Y, Zhang X, Wu Y, Wang Q, Yang S World J Clin Cases. 2022; 10(35):12996-13005.

PMID: 36569010 PMC: 9782930. DOI: 10.12998/wjcc.v10.i35.12996.


Thrombosis in Inherited Fibrinogen Disorders.

Korte W, Poon M, Iorio A, Makris M Transfus Med Hemother. 2017; 44(2):70-76.

PMID: 28503122 PMC: 5425758. DOI: 10.1159/000452864.


Hematopoietic stem cell transplantation for Hodgkin's disease in a patient with dysfibrinogenemia and thrombosis.

Ganti A, Vose J, Haire W J Thromb Thrombolysis. 2006; 23(2):155-8.

PMID: 17131175 DOI: 10.1007/s11239-006-9037-0.