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A Case Report of Congenital Afibrinogenemia

Year 2014, Volume: 1 Issue: 1, 27 - 30, 01.03.2014

Abstract

Congenital afibrinogenemia is a rare bleeding disorder. It may be manifested as umblical, mucosal, intramuscular, intraarticular, or life-threatening intracranial bleeding. A third-day-old infant was admitted for umblical cord bleeding, and was found to have a prolonged prothrobin time [PT], and activated partial thromboplastin time [aPTT], and a very low fibrinogen level. He was diagnosed as congenital afibrinogenemia, and reported for the rarity of disease, and discussion of novel therapeutic approaches

References

  • Conflict of Interest
  • The authors declared that they had no
  • anaesthesiology. 2008;25(6):519-21. European journal of 14.
  • Cronin C, Fitzpatrick D, Temperley I. Multiple pulmonary
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  • De Mattia D, Regina G, Giordano P, Del Vecchio GC,
  • Altomare M, Schettini F. Association of congenital
  • afibrinogenemia and K-dependent protein C deficiency--a
  • case report. Angiology. 1993;44(9):745-9. 16. de Moerloose P, Neerman-Arbez M. Congenital fibrinogen disorders. Seminars in thrombosis and hemostasis. 2009;35(4):356-66. 17. Peyvandi F, Haertel S, Knaub S, Mannucci PM. Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia. Journal of thrombosis and haemostasis : JTH. 2006;4(7):1634-7. 18.
  • Parameswaran R, Dickinson JP, de Lord S, Keeling DM,
  • Colvin BT. Spontaneous intracranial bleeding in two
  • patients with congenital afibrinogenaemia and the role of
  • replacement therapy. Haemophilia : the official journal of
  • the World Federation of Hemophilia. 2000;6(6):705-8.
  • Copyright © 2014 The Author(s); This is an open-access article distributed under the terms of the Creative Commons Attribution
  • License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium,
  • provided the original work is properly cited.
Year 2014, Volume: 1 Issue: 1, 27 - 30, 01.03.2014

Abstract

References

  • Conflict of Interest
  • The authors declared that they had no
  • anaesthesiology. 2008;25(6):519-21. European journal of 14.
  • Cronin C, Fitzpatrick D, Temperley I. Multiple pulmonary
  • emboli in a patient with afibrinogenaemia. Acta
  • haematologica. 1988;79(1):53-4. 15.
  • De Mattia D, Regina G, Giordano P, Del Vecchio GC,
  • Altomare M, Schettini F. Association of congenital
  • afibrinogenemia and K-dependent protein C deficiency--a
  • case report. Angiology. 1993;44(9):745-9. 16. de Moerloose P, Neerman-Arbez M. Congenital fibrinogen disorders. Seminars in thrombosis and hemostasis. 2009;35(4):356-66. 17. Peyvandi F, Haertel S, Knaub S, Mannucci PM. Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia. Journal of thrombosis and haemostasis : JTH. 2006;4(7):1634-7. 18.
  • Parameswaran R, Dickinson JP, de Lord S, Keeling DM,
  • Colvin BT. Spontaneous intracranial bleeding in two
  • patients with congenital afibrinogenaemia and the role of
  • replacement therapy. Haemophilia : the official journal of
  • the World Federation of Hemophilia. 2000;6(6):705-8.
  • Copyright © 2014 The Author(s); This is an open-access article distributed under the terms of the Creative Commons Attribution
  • License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium,
  • provided the original work is properly cited.
There are 18 citations in total.

Details

Primary Language English
Journal Section Case Reports
Authors

Aysen Turedi Yildirim This is me

Gokmen Bilgili This is me

Ozlem Buga This is me

Ozen Tekin This is me

Huseyin Gulen This is me

Publication Date March 1, 2014
Published in Issue Year 2014 Volume: 1 Issue: 1

Cite

APA Yildirim, A. T., Bilgili, G., Buga, O., Tekin, O., et al. (2014). A Case Report of Congenital Afibrinogenemia. Medical Science and Discovery, 1(1), 27-30. https://doi.org/10.17546/msd.81571
AMA Yildirim AT, Bilgili G, Buga O, Tekin O, Gulen H. A Case Report of Congenital Afibrinogenemia. Med Sci Discov. March 2014;1(1):27-30. doi:10.17546/msd.81571
Chicago Yildirim, Aysen Turedi, Gokmen Bilgili, Ozlem Buga, Ozen Tekin, and Huseyin Gulen. “A Case Report of Congenital Afibrinogenemia”. Medical Science and Discovery 1, no. 1 (March 2014): 27-30. https://doi.org/10.17546/msd.81571.
EndNote Yildirim AT, Bilgili G, Buga O, Tekin O, Gulen H (March 1, 2014) A Case Report of Congenital Afibrinogenemia. Medical Science and Discovery 1 1 27–30.
IEEE A. T. Yildirim, G. Bilgili, O. Buga, O. Tekin, and H. Gulen, “A Case Report of Congenital Afibrinogenemia”, Med Sci Discov, vol. 1, no. 1, pp. 27–30, 2014, doi: 10.17546/msd.81571.
ISNAD Yildirim, Aysen Turedi et al. “A Case Report of Congenital Afibrinogenemia”. Medical Science and Discovery 1/1 (March 2014), 27-30. https://doi.org/10.17546/msd.81571.
JAMA Yildirim AT, Bilgili G, Buga O, Tekin O, Gulen H. A Case Report of Congenital Afibrinogenemia. Med Sci Discov. 2014;1:27–30.
MLA Yildirim, Aysen Turedi et al. “A Case Report of Congenital Afibrinogenemia”. Medical Science and Discovery, vol. 1, no. 1, 2014, pp. 27-30, doi:10.17546/msd.81571.
Vancouver Yildirim AT, Bilgili G, Buga O, Tekin O, Gulen H. A Case Report of Congenital Afibrinogenemia. Med Sci Discov. 2014;1(1):27-30.