A Case Report of Congenital Afibrinogenemia

Cilt: 1 Sayı: 1 1 Mart 2014
  • Aysen Turedi Yildirim
  • Gokmen Bilgili
  • Ozlem Buga
  • Ozen Tekin
  • Huseyin Gulen
Medical Science and Discovery Kapak
Medical Science and Discovery
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A Case Report of Congenital Afibrinogenemia

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

Keywords

Kaynakça

  1. Conflict of Interest
  2. The authors declared that they had no
  3. anaesthesiology. 2008;25(6):519-21. European journal of 14.
  4. Cronin C, Fitzpatrick D, Temperley I. Multiple pulmonary
  5. emboli in a patient with afibrinogenaemia. Acta
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  7. De Mattia D, Regina G, Giordano P, Del Vecchio GC,
  8. Altomare M, Schettini F. Association of congenital

Ayrıntılar

Birincil Dil

İngilizce

Konular

-

Bölüm

-

Yazarlar

Aysen Turedi Yildirim Bu kişi benim

Gokmen Bilgili Bu kişi benim

Ozlem Buga Bu kişi benim

Ozen Tekin Bu kişi benim

Huseyin Gulen Bu kişi benim

Yayımlanma Tarihi

1 Mart 2014

Gönderilme Tarihi

26 Aralık 2014

Kabul Tarihi

-

Yayımlandığı Sayı

Yıl 2014 Cilt: 1 Sayı: 1

DOI

https://doi.org/10.17546/msd.81571

IZ

https://izlik.org/JA64EH47FB

Kaynak Göster

RIS / Bibtex
APA
Yildirim, A. T., Bilgili, G., Buga, O., Tekin, O., & Gulen, H. (2014). A Case Report of Congenital Afibrinogenemia. Medical Science and Discovery, 1(1), 27-30. https://doi.org/10.17546/msd.81571
AMA
1.Yildirim AT, Bilgili G, Buga O, Tekin O, Gulen H. A Case Report of Congenital Afibrinogenemia. Med Sci Discov. 2014;1(1):27-30. doi:10.17546/msd.81571
Chicago
Yildirim, Aysen Turedi, Gokmen Bilgili, Ozlem Buga, Ozen Tekin, ve Huseyin Gulen. 2014. “A Case Report of Congenital Afibrinogenemia”. Medical Science and Discovery 1 (1): 27-30. https://doi.org/10.17546/msd.81571.
EndNote
Yildirim AT, Bilgili G, Buga O, Tekin O, Gulen H (01 Mart 2014) A Case Report of Congenital Afibrinogenemia. Medical Science and Discovery 1 1 27–30.
IEEE
[1]A. T. Yildirim, G. Bilgili, O. Buga, O. Tekin, ve H. Gulen, “A Case Report of Congenital Afibrinogenemia”, Med Sci Discov, c. 1, sy 1, ss. 27–30, Mar. 2014, doi: 10.17546/msd.81571.
ISNAD
Yildirim, Aysen Turedi - Bilgili, Gokmen - Buga, Ozlem - Tekin, Ozen - Gulen, Huseyin. “A Case Report of Congenital Afibrinogenemia”. Medical Science and Discovery 1/1 (01 Mart 2014): 27-30. https://doi.org/10.17546/msd.81571.
JAMA
1.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, vd. “A Case Report of Congenital Afibrinogenemia”. Medical Science and Discovery, c. 1, sy 1, Mart 2014, ss. 27-30, doi:10.17546/msd.81571.
Vancouver
1.Aysen Turedi Yildirim, Gokmen Bilgili, Ozlem Buga, Ozen Tekin, Huseyin Gulen. A Case Report of Congenital Afibrinogenemia. Med Sci Discov. 01 Mart 2014;1(1):27-30. doi:10.17546/msd.81571