Clinical and genetic spectrum of factor XII deficiency in the Han population of East China [PDF]
Orphanet Journal of Rare DiseasesBackground Factor XII (FXII or F12) deficiency is a rare inherited disorder, typically lacking haemorrhagic symptoms. There is limited literature exists on FXII deficiency and mutations within the Chinese population.
Fei Xu +5 more
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Safety of Tonsillectomy and/or Adenoidectomy in Pediatric Patients with Prolonged Activated Partial Thromboplastin Time and Factor XII Deficiency [PDF]
Journal of Inflammation ResearchJun Du,1 Qing-long Gu,1 Ying-xia Lu,1 Lei Zhang,2 Xiao-jun Zhan,1 Zhan Wang1 1Department of Otolaryngology, Head and Neck Surgery, Children’s Hospital Capital Institute of Pediatrics, Beijing, 100000, People’s Republic of China; 2Department of ...
Du J +5 more
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Point-of-care ClotPro thromboelastography to determine bleeding risk in two cats with factor XII deficiency [PDF]
Journal of Feline Medicine and Surgery Open ReportsCase series summary Factor XII (FXII) deficiency is a rare autosomal recessive genetic disorder in cats, leading to singular prolonged activated partial thromboplastin clotting time (aPTT) without increased bleeding risk.
Vera Forer +5 more
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Cardiopulmonary Bypass in a Patient with Factor XII Deficiency. [PDF]
J Extra Corpor Technol, 2014 The performance of cardiopulmonary bypass (CPB) in the factor XII-deficient patient is challenging in that the normal method for monitoring anticoagulation is ineffective as a result of an impaired contact activation system. We report the case of a factor XII-deficient patient who underwent surgical revascularization on CPB.
Cronbaugh RD +3 more
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Novel mutations in congenital factor XII deficiency
Frontiers in Bioscience - Landmark, 2016 Several mutations in factor XII have been reported in patients with factor XII deficiency. Here, we described three mutations in the F12 gene (c. 6635G more than A (p. G259E), c. 6658G more than C (p. R267G) and c. 8489G more than A (p. E521K)) of five patients with congenital FXII deficiency. Among these, two were heterozygous mutations.
Xi Mo, Xuefeng Wang, Hui Yan
exaly +3 more sources
A novel missense mutation in the factor XII gene in a litter of cats with factor XII deficiency. [PDF]
J Vet Med Sci, 2017 The feline F12 gene was examined to identify a mutation associated with coagulation factor XII (FXII) deficiency in a litter of 6 cats, including 2 cats with severely reduced FXII activity (7.1 and 9.3%, respectively) and 4 cats with moderately reduced FXII activity (range 36.0 to 46.3%). Cats with severely reduced FXII activity were homozygous for a G
Maruyama H +4 more
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Acquired factor XII deficiency following transanal excision of rectal lesion by transanal minimally invasive surgery (TAMIS): a case report and literature review [PDF]
World Journal of Surgical Oncology, 2018 Background Local excision (LE) is currently one of the most effective methods used in cases of large benign polyps, not suitable for endoscopic treatment, or early-stage neoplasms.
Maria Rita Cozzi +3 more
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Transient acquired factor XII deficiency associated with moderately severe Covid-19 pneumonia [PDF]
Hematology, Transfusion and Cell Therapy, 2021 Nigel P. Murray +2 more
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Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation [PDF]
International Journal of Hematology, 2022 Ming-Ching Shen +2 more
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Factor XII deficiency in asymptomatic Saudi population: A retrospective cohort study [PDF]
Saudi Journal of Biological Sciences, 2021 Farjah Algahtani, Fatmah S Alqahtany
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