Advanced search
Publication Cover
Hematology Volume 24, 2019 - Issue 1
Submit an article Journal homepage
3,601
Views
6
CrossRef citations to date
0
Altmetric
Articles

Factor VII deficiency – an enigma; clinicohematological profile in 12 cases

Preeti TripathiDepartment of Hematology, All India Institute of Medical Sciences, New Delhi, India
,
Priyanka MishraDepartment of Hematology, All India Institute of Medical Sciences, New Delhi, IndiaCorrespondence[email protected]
,
Ravi RanjanDepartment of Hematology, All India Institute of Medical Sciences, New Delhi, India
,
Seema TyagiDepartment of Hematology, All India Institute of Medical Sciences, New Delhi, India
,
Tulika SethDepartment of Hematology, All India Institute of Medical Sciences, New Delhi, India
&
Renu SaxenaDepartment of Hematology, All India Institute of Medical Sciences, New Delhi, India
Pages 97-102 | Published online: 07 Sep 2018

References

  • Perry DJ. Factor VII deficiency – a review. Br J Haematol. 2002;118:689–700. doi: 10.1046/j.1365-2141.2002.03545.x
  • Ingerslev J, Christiansen K, Sørensen B; International Registry on Factor VII Deficiency (IRF7) Steering Committee. Inhibitor to factor VII in severe factor VII deficiency: detection and course of the inhibitory response. J Thromb Haemost. 2005;3:799–800. doi: 10.1111/j.1538-7836.2005.01225.x
  • Napolitano M, Giansily-Blaizot M, Dolce A, et al. Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. results from the Seven Treatment Evaluation Registry (STER). Haematologica. 2013;98:538–544. doi: 10.3324/haematol.2012.074039
  • Bladbjerg EM, Gram J, Jespersen J. Plasma concentrations of blood coagulation factor VII measured by immunochemical and amidolytic methods. Scand J Clin Lab Invest. 2000;60:161–168. doi: 10.1080/003655100750044802
  • Wildgoose P, Nemerson Y, Hansen LL, et al. Measurement of basal levels of factor VIIa in hemophilia A and B patients. Blood. 1992;80:25–28.
  • Peyvandi F, Mannucci PM, Asti D, et al. Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency. Haemophilia. 1997;3:242–246. doi: 10.1046/j.1365-2516.1997.00137.x
  • Marty S, Barro C, Chatelain B, et al. The paradoxical association between inherited factor VII deficiency and venous thrombosis. Haemophilia. 2008;14:564–570. doi: 10.1111/j.1365-2516.2007.01647.x
  • Napolitano M, Siragusa S, Mariani G. Factor VII deficiency: clinical phenotype, genotype and therapy. J Clin Med. 2017;38:1–8.
  • Herrmann FH, Wulff K, Auberger K, et al. Molecular biology and clinical manifestation of hereditary factor VII deficiency. Semin Thromb Hemost. 2000;26:393–400. doi: 10.1055/s-2000-8458
  • Rao G, Viswabandya A, Nair SC, et al. Molecular basis of hereditary factor VII deficiency in India: five novel mutations including a double missense mutation (Ala191Glu; Trp364Cys) in 11 unrelated patients. Haematologica. 2007;92:1002–1003. doi: 10.3324/haematol.10835
  • Bernardi F, Castaman G, Pinotti M, et al. Mutation pattern in clinically asymptomatic coagulation factor VII deficiency. Hum Mutat. 1996;8:108–115. doi: 10.1002/(SICI)1098-1004(1996)8:2<108::AID-HUMU2>3.0.CO;2-7
  • Feng D, Tofler GH, Larson MG, et al. Factor VII gene polymorphism, factor VII levels, and prevalent cardiovascular disease: the Framingham Heart Study. Arterioscler Thromb Vasc Biol. 2000;20:593–600. doi: 10.1161/01.ATV.20.2.593
  • Mariani G, Konkle BA, Ingerslev J. Congenital factor VII deficiency: therapy with recombinant activated factor VII – a critical appraisal. Haemophilia. 2006;12:19–27. doi: 10.1111/j.1365-2516.2006.01180.x
  • Gralnick HR, Wilson OJ. Cold-promoted activation of factor VII and shortening of the prothrombin time. In: Wessler S, Becker CG, Nemerson Y, editors. The new dimensions of warfarin prophylaxis. Boston (MA): Springer; 1987. p. 113–129.
  • Lapecorella M, Mariani G; International Registry on Congenital Factor VII Deficiency. Factor VII deficiency: defining the clinical picture and optimizing therapeutic options. Haemophilia. 2008;14(6):1170–1175. doi: 10.1111/j.1365-2516.2008.01844.x
  • Mariani G, Herrmann FH, Dolce A, et al. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost. 2005;93(3):481–487.
  • Palla R, Peyvandi F, Shapiro AD. Rare bleeding disorders: diagnosis and treatment. Blood. 2015;125:2052–2061. doi: 10.1182/blood-2014-08-532820
  • Millar DS, Kemball-Cook G, McVey JH, et al. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency. Hum Genet. 2000;107(4):327–342. doi: 10.1007/s004390000373
  • Girolami A, Bertozzi I, Berti de Marinis G, et al. Activated FVII levels in factor VII Padua (Arg304Gln) coagulation disorder and in true factor VII deficiency: a study in homozygotes and heterozygotes. Hematology. 2011;16:308–312. doi: 10.1179/102453311X13085644680069
  • Matteo NDM, Mariani G (on behalf of STER study group). Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency. Thromb Haemost. 2013;109:1051–1059. doi: 10.1160/TH12-10-0740

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.