Article
Factor XIII deficiency in south of Tunisia.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Sept 2017
Maaloul Ines, Medhaffer Moez, Louhichi Nacim, Krichen Imen, Alibi Sofien, Kmiha Sana, Aloulou Hajer, Fakhfakh Faiza, Elloumi Moez, Kallel Choumous, Hachicha Mongia
Abstract excerpt
: Factor XIII deficiency is a rare autosomal recessive disorder of hemostasis characterized by a plasmatic factor XIII level less than 1% in homozygote and bleeding as of the youth. The aim of the study is to describe the clinical features and the outcome of the patients and to determine molecular characteristics. A retrospective study, was conducted on seven patients with factor XIII deficiency in the department...
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