Hemophilia B

Hemophilia B is a form of hemophilia (see this term) characterized by spontaneous or prolonged hemorrhages due to factor IX deficiency.

Shock

The state in which profound and widespread reduction of effective tissue perfusion leads first to reversible, and then if prolonged, to irreversible cellular injury.


Total: 2

                       


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PMID (PMCID)
20093865
 MIXED_SAMPLE Infant, Newborn
Perinatal hemorrhagic shock after fetal scalp blood sampling.
Sabir H, Stannigel H, Schwarz A, Hoehn T.
Obstet Gynecol. 2010;115(2 Pt 2):419-20.
The underlying reason for the development of hemorrhagic shock was factor IX-deficiency resulting from spontaneous mutation.
8515646
 MALE Adult
[Extracorporeal shock wave lithotripsy in a patient with hemophilia B].
Yokoyama T, Nasu Y.
Nihon Hinyokika Gakkai Zasshi. 1993;84(3):566-9.
[Extracorporeal shock wave lithotripsy in a patient with hemophilia B].