A Case Report of Congenital Afibrinogenemia
Journal Title: Medical Science and Discovery - Year 2014, Vol 1, Issue 1
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
Authors and Affiliations
Aysen Turedi Yildirim, Gokmen Bilgili, Ozlem Buga, Ozen Tekin, Huseyin Gulen
Keywords
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