1.
Ann Biol Clin (Paris)
; 68(5): 595-7, 2010.
Article
in French
| MEDLINE
| ID: mdl-20870582
ABSTRACT
The deficiency in factor I or fibrinogen is a largely unknown genetic disease. It is a rare condition inherited as an autosomal recessive, whose clinical events are variable, ranging from moderate to minimal bleeding or cataclysmic hemorrhage. We report a case of congenital afibrinogenemia in a 17 years-old patient hospitalized in surgical ICU for hemoperitoneum medium abundance discovered by abdominal ultrasound performed before a picture of abdominopelvic pain lasting for 24 hours. Exploration led to the diagnosis of congenital afibrinogenemia with favorable evolution with a contribution of factor deficient. Through this case we raise the problem of congenital afibrinogenemia in diagnosis and the peculiarities of its management.
Subject(s)
Afibrinogenemia/congenital , Hemoperitoneum/genetics , Adolescent , Afibrinogenemia/genetics , Afibrinogenemia/therapy , Blood Transfusion , Female , Hemoperitoneum/diagnosis , Hemoperitoneum/therapy , Humans
2.
Tunis Med
; 90(7): 589-90, 2012 Jul.
Article
in French
| MEDLINE
| ID: mdl-22811239