A Novel Phenotype of the Factor 5 Gene Mutation (Homozygote Met1736Val and Heterozygote Asp68His) Is Associated With Moderate Factor V Deficiency [PDF]
Frontiers in Medicine, 2022 BackgroundFactor V (FV) deficiency is a rare disease, with a low incidence rate in Asia. Therefore, the F5 mutation in the Taiwanese population is poorly understood.MethodsA Chinese family with FV deficiency was included, and the patient and his family ...
Yueh-Shih Chang +8 more
doaj +4 more sources
Fatal acquired coagulation factor V deficiency after hepatectomy for advanced hepatocellular carcinoma as a possible immune checkpoint inhibitor-related adverse event: a case report [PDF]
Surgical Case Reports, 2023 Background Atezolizumab plus bevacizumab therapy was recently introduced as the first line for unresectable advanced hepatocellular carcinoma (HCC), but immune-related adverse events (IrAEs) due to atezolizumab are a great concern.
Shintaro Arakaki +13 more
doaj +4 more sources
Refractory Epistaxis due to Severe Factor V Deficiency with Inhibitor [PDF]
Case Reports in Hematology, 2015 Factor V deficiency secondary to inhibitors is extremely rare and can be caused by a wide collection of exposures such as bovine thrombin and beta lactamase antibiotics. The management of factor V deficiency with inhibitor is a condition treated based on
Elizabeth S. John +2 more
doaj +4 more sources
Massive Intramuscular Haematoma Due to Acquired Factor V Deficiency [PDF]
eJHaemLara Budwig +5 more
doaj +4 more sources
Recurrent miscarriage in a woman with congenital factor V deficiency: a case report [PDF]
BMC Pregnancy and Childbirth, 2022 Background Factor V deficiency is a rare bleeding disorder that can be either congenital or acquired. Factor V deficiency mostly present with mucosal bleeding. Coagulation factor V does not increase considerably during normal gestation.
Mohammad Shirzadi +2 more
doaj +2 more sources
Case Report: Novel Mutation of F5 With Maternal Uniparental Disomy Causes Severe Congenital Factor V Deficiency [PDF]
Frontiers in Pediatrics, 2022 We summarized two cases of congenital factor V deficiency (FVD) associated with a novel F5 mutation, and analyzed the relationship of the clinical features and genetic characteristics in congenital FVD.
Lin Cheng, Ying Li, Wenjuan Zhou, Tao Bo
doaj +2 more sources
Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report [PDF]
Journal of Medical Case Reports, 2023 Background Hemophilia is an X-linked, recessive inherited disease caused by a defect or deficiency of one of the coagulation factors (VIII or IX). It is considered a rare disease in females.
Rawan Al khudari +3 more
doaj +2 more sources
Laparoscopic hepatectomy for hepatocellular carcinoma in a patient with congenital factor V deficiency: a case report [PDF]
Surgical Case Reports, 2022 Background Factor V (FV) deficiency is an extremely rare disease, with an incidence of 1 in 1 million. The bleeding symptoms are mild, and the prognosis is good; however, the safety of surgical treatment is unclear, because there are few available ...
Takaomi Seki +12 more
doaj +2 more sources
Congenital Factor V deficiency: perioperative management (case report) [PDF]
The Pan African Medical Journal, 2020 Factor V congenital deficiency is a rare hereditary disease, it exposes patients to hemorrhagic risk, with high morbi-mortality. Its management is a real challenge for practitioners.
Mohamed Anass Fehdi +5 more
doaj +2 more sources
Acquired factor V deficiency in an elderly hemodialysis patient: a case report and literature review [PDF]
BMC NephrologyBackground Acquired factor V deficiency (AFVD) is a rare hemorrhagic disorder caused by autoantibodies against coagulation factor V. Clinical manifestations vary widely, ranging from asymptomatic cases to severe hemorrhage or even thrombosis, and ...
Ayaka Hane +6 more
doaj +2 more sources