As the third most common vascular disease, venous thromboembolism is associated with
significant mortality and morbidity. Pathogenesis underlying venous thrombosis is still not …

Factor XIII deficiency (FXIIID) is a rare hereditary bleeding disorder arising from
heterogeneous mutations, which can lead to life‐threatening hemorrhage. The diagnosis of …

Factor XIII (FXIII) deficiency is an extremely rare hemorrhagic disorder with an approximate
worldwide incidence of one per two million. With current tests, diagnosis of this disease can …

Intracranial hemorrhage (ICH) is a medical emergency. In congenital bleeding disorders,
ICH is a devastating presentation accompanied with a high rate of morbidity and mortality …

Factor XIII (FXIII) is a protein involved in blood clot stabilisation which also plays an
important role in processes including trauma, wound healing, tissue repair, pregnancy, and …

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Background Retinal hemorrhages (RH) are a common manifestation of abusive head
trauma (AHT) resulting from acceleration-deceleration injury with or without blunt impact …

Factor XIII deficiency (FXIIID) is an extremely rare autosomal recessive disorder that has the
highest incidence in Iran. The FXIIID is primarily due to mutations in the FXIII-A gene, most of …

Congenital bleeding disorders (CBDs) are a heterogeneous group of disorders with variable
clinical presentations ranging from asymptomatic conditions, mostly in inherited platelet …

Introduction Fibrin stabilizing factor (FXIII) plays a crucial role in blood clotting, tissue repair,
and immune defense. FXIII deficiency after trauma can lead to prolonged wound healing …