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Congenital Bleeding Disorder

Known as: Congenital Bleeding Defect, Congenital Coagulation Defect 
A bleeding disorder that is diagnosed during childhood, with the presenting symptom of excessive bleeding.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
&NA; Intracranial hemorrhage (ICH), as a life-threatening bleeding among all kinds of congenital bleeding disorders (CBDs), is a… Expand
Review
2006
Review
2006
OBJECTIVE The prevalence of bleeding disorders, notably von Willebrand disease (vWD), among adult women with objectively… Expand
Review
2005
Review
2005
  • M. Cattaneo
  • Seminars in thrombosis and hemostasis
  • 2005
  • Corpus ID: 25392151
Platelets possess three P2 receptors: two (P2Y (1) and P2Y (12)) are receptors for adenosine diphosphate (ADP), and one (P2X1) is… Expand
Review
2003
Review
2003
Both clinical and basic problems related to the congenital bleeding disorders continue to confront hematologists. On the… Expand
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Highly Cited
2001
Highly Cited
2001
Upshaw-Schulman syndrome (USS) is a congenital bleeding disorder characterized by repeated episodes of thrombocytopenia and… Expand
Highly Cited
2001
Highly Cited
2001
The gray platelet syndrome (GPS) is a rare congenital bleeding disorder in which thrombocytopenia is associated with increased… Expand
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Highly Cited
1998
Highly Cited
1998
Treatment of a Patient with Bernard-Soulier Syndrome and Recurrent Nosebleeds with Recombinant VIIa - 
Highly Cited
1990
Highly Cited
1990
We have studied a patient with a congenital bleeding disorder and phenotypic manifestations typical of Bernard-Soulier syndrome… Expand
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1970
1970
A 23-year-old white male with a bleeding tendency since early childhood presented a congenital coagulation defect similar but not… Expand
Review
1969
Review
1969
  • E. R. Olsen
  • Archives of neurology
  • 1969
  • Corpus ID: 38731818
CLASSIC hemophilia is a congenital coagulation defect caused by an absence or low concentration of the plasma protein factor VIII… Expand