Hemophilia is a bleeding diathesis that inhibits proper hemostasis. The most common type of hemophilia is "Hemophilia A, or classic hemophilia," a condition manifested by a deficiency of factor VIII. Females may be carriers of the factor VIII gene deficiency increasing their risk of bleeding. Neuraxial anesthesia has been proven to be a safe procedure and provides adequate pain control while decreasing morbidity and mortality in the obstetric population. Case presented is a parturient scheduled for cesarean section of full-term twins that is a carrier of hemophilia A. This case represents the involvement of a multidisciplinary team including obstetrician, anesthetist, and hematologist identifying optimal treatment for this patient. The admi...
International audienceThe optimal mode of delivery for a pregnant hemophilia carrier is still a matt...
The optimal mode of delivery for a pregnant hemophilia carrier is still a matter of debate. The aim ...
Hyperhomocysteinemia is due to genetic and acquired changes in the metabolism of homocysteine. It is...
Hemophilia A carriers are usually asymptomatic and their risk of bleeding when giving birth is not n...
SummaryBackground and objectivesFactor XI deficiency is a rare hematologic disorder. Hemophilia C (f...
Neuraxial anesthesia, as the standard of care for Cesarean deliveries, is associated with decreased ...
Hemophilia A is a hemorrhagic trend almost exclusively affecting males (X-related recessive disease)...
Hemophilia is mostly an inherited genetic disorder, caused by mutations in the clotting factor gene....
Study Design Single-center retrospective study. Purpose To optimize the perioperative management of ...
Hemophilia presents challenging consideration for anesthesiologists. In non emergency cases it is es...
Factor XI deficiency is a hereditary blood coagulation disorders. Puerpera with factor XI deficiency...
Hemophilia B is a coagulation disorder characterized by a deficiency of clotting factor IX. Women ar...
Hemophilia A and B are the best known of the hereditary bleeding disorders. Hemophilia A and B are X...
Haemofilia A is congenital blood disease with female carrier, usualy found in male patient and happe...
HELLP syndrome is characterized by hemolysis, elevated liver enzymes and thrombocytopenia. It may ca...
International audienceThe optimal mode of delivery for a pregnant hemophilia carrier is still a matt...
The optimal mode of delivery for a pregnant hemophilia carrier is still a matter of debate. The aim ...
Hyperhomocysteinemia is due to genetic and acquired changes in the metabolism of homocysteine. It is...
Hemophilia A carriers are usually asymptomatic and their risk of bleeding when giving birth is not n...
SummaryBackground and objectivesFactor XI deficiency is a rare hematologic disorder. Hemophilia C (f...
Neuraxial anesthesia, as the standard of care for Cesarean deliveries, is associated with decreased ...
Hemophilia A is a hemorrhagic trend almost exclusively affecting males (X-related recessive disease)...
Hemophilia is mostly an inherited genetic disorder, caused by mutations in the clotting factor gene....
Study Design Single-center retrospective study. Purpose To optimize the perioperative management of ...
Hemophilia presents challenging consideration for anesthesiologists. In non emergency cases it is es...
Factor XI deficiency is a hereditary blood coagulation disorders. Puerpera with factor XI deficiency...
Hemophilia B is a coagulation disorder characterized by a deficiency of clotting factor IX. Women ar...
Hemophilia A and B are the best known of the hereditary bleeding disorders. Hemophilia A and B are X...
Haemofilia A is congenital blood disease with female carrier, usualy found in male patient and happe...
HELLP syndrome is characterized by hemolysis, elevated liver enzymes and thrombocytopenia. It may ca...
International audienceThe optimal mode of delivery for a pregnant hemophilia carrier is still a matt...
The optimal mode of delivery for a pregnant hemophilia carrier is still a matter of debate. The aim ...
Hyperhomocysteinemia is due to genetic and acquired changes in the metabolism of homocysteine. It is...