Author:
Yildirim Aysen Turedi,Bilgili Gokmen,Buga Ozlem,Tekin Ozen,Gulen Huseyin
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
Subject
General Earth and Planetary Sciences,General Environmental Science
Cited by
1 articles.
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