Open Journal of Blood Diseases

Volume 5, Issue 4 (December 2015)

ISSN Print: 2164-3180   ISSN Online: 2164-3199

Google-based Impact Factor: 0.56  Citations  

Factor XII (Hageman Factor) Deficiency: A Very Rare Coagulation Disorder

HTML  XML Download Download as PDF (Size: 338KB)  PP. 39-42  
DOI: 10.4236/ojbd.2015.54006    4,950 Downloads   8,210 Views  Citations

ABSTRACT

Background: Factor XII (Hageman Factor) is the initiating factor for the Intrinsic Pathway of Coagulation. Very low levels of Factor XII have been associated with increased levels of activated Partial Thromboplastin Time (aPTT). Association of Factor XII deficiency is more with thromboembolic disorders rather than bleeding tendencies. Aim: To learn more about the relationship of factor XII (Hageman Factor) deficiency and high levels of activated Partial Thromboplastin Time. Case Presentation: The Patient was admitted with complains of recurrent headaches and loin pain. Patient was incidentally found to have prolonged activated Partial Thromboplastin Time. This led to investigations which ultimately provided the evidence of severely low levels of Hageman Factor. Conclusion: Hageman Factor deficiency causes prolonged activated Partial Thromboplastin Time. However, most of the patients are asymptomatic for many years despite Hageman Factor deficiency.

Share and Cite:

Azaad, M. , Zhang, Q. and Li, Y. (2015) Factor XII (Hageman Factor) Deficiency: A Very Rare Coagulation Disorder. Open Journal of Blood Diseases, 5, 39-42. doi: 10.4236/ojbd.2015.54006.

Cited by

[1] An unanticipated prolonged baseline ACT during cardiac surgery due to factor XII deficiency
Annals of Cardiac …, 2022
[2] Hereditary factor XII deficiency in an adult patient: A case report
Ansari, F Al-Yami, G Almulhim… - SAGE Open Medical …, 2022
[3] Unusual Presentation of Factor XII Deficiency with Bleeding: A Rare Case Report: LMRJ
LIAQUAT MEDICAL RESEARCH JOURNAL, 2020
[4] Unusual Presentation of Factor XII Deficiency with Bleeding: A Rare Case Report
2020
[5] A PATIENT WITH FXII DEFICIENCY, JAK2-MUTATION POSITIVE CHRONIC MYELOPROLIFERATIVE NEOPLASM AND RECURRENT THROMBOEMBOLIC EVENTS
2019
[6] Korelasi antara Kadar Faktor XII dengan Plasmin Serum pada Pasien Sindroma Koroner Akut
2019
[7] BOLESNICA S MANJKOM FXII, JAK2-MUTACIJA POZITIVNOM KRONIČNOM MIJELOPROLIFERATIVNOM NEOPLAZMOM I PONAVLJANIM ROMBOEMBOLIJSKIM …
Acta medica Croatica: Časopis …, 2019
[8] A PATIENT WITH FXII DEFICIENCY, JAK2-MUTATION POSITIVE CHRONIC MYELOPROLIFERATIVE NEOPLASM AND RECURRENT THROMBOEMBOLIC …
Acta medica Croatica: Časopis Akademije …, 2019
[9] A Rare Case of Symptomatic Factor XII Deficiency Manifesting as Intraventricular Haemorrhage and Hydrocephalus in a Term Neonate
2018
[10] Pathophysiology of bleeding diathesis in haemophilia-A: a sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic …
Egyptian Journal of Medical Human Genetics, 2018
[11] Factor XII Deficiency Mimicking Bleeding Diathesis: A Unique Presentation and Diagnostic Pitfall
2018
[12] Acquired Hemophilia of Unknown Etiology in an Elderly Man: Case Report
The American journal of case reports, 2018
[13] Krešėjimo kaskados vidinės aktyvacijos kelio sutrikimų ir laboratorinės diagnostikos ryšys.
Thesis, 2017
[14] Intrinsic coagulation pathway disorders and laboratory diagnostic correlations.
2017

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.