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Dysfibrinogenemia, Congenital

Known as: CONGENITAL DYSFIBRINOGENEMIA 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

AfibrinogenemiaDysfibrinogenemia
Congenital hypofibrinogenemia

Papers overview

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Review
2020
Review
2020
Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia
Congenital dysfibrinogenemia (CD) is a rare disorder of hemostasis. The majority of cases are caused by heterozygous missense… 
2016
2016
Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His
AbstractCongenital dysfibrinogenemia (CD) is a qualitative fibrinogen disorder caused by an abnormal fibrinogen molecule… 
Highly Cited
2015
Highly Cited
2015
Natural history of patients with congenital dysfibrinogenemia.
We conducted a multicenter study of 101 patients with congenital dysfibrinogenemia (CD) to characterize the incidence of… 
2009
2009
Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen.
Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in… 
2005
2005
Stroke in two young siblings with congenital dysfibrinogenemia
Two young siblings (a male of 21 and his sister of 26 years) suffered from arterial thrombosis episodes of the carotid and… 
Review
2002
Review
2002
Dysfibrinogenemia and thrombosis.
  • T. Hayes
  • Archives of pathology & laboratory medicine
  • 2002
  • Corpus ID: 30198106
OBJECTIVES To review the state of the art relating to congenital dysfibrinogenemia as a potential risk factor for thrombosis, as… 
1992
1992
Severe congenital dysfibrinogenemia (fibrinogen-Riyadh): a family study.
Congenital severe dysfibrinogenemia was discovered in a small Saudi family. Their single child exhibited abnormal severe bleeding… 
1988
1988
Fibrinogen Baltimore III: congenital dysfibrinogenemia with a shortened gamma-subunit.
An abnormal fibrinogen has been found in an asymptomatic Negro female. Clinical laboratory findings were normal, except for a… 
Highly Cited
1983
Highly Cited
1983
Hereditary dysfibrinogenemia in a patient with thrombotic disease
A new case of congenital dysfibrinogenemia, in which the patient has severe thrombotic disease, is reported. The abnormal… 
Highly Cited
1971
Highly Cited
1971
Fibrinogen Bethesda: a congenital dysfibrinogenemia with delayed fibrinopeptide release.
A dysfibrinogenemia (fibrinogen Bethesda) was detected in a 9 yr old male of Mexican-English extraction who had a lifelong… 
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