Factor XIII (FXIII) is a multifunctional pro-γ-transglutaminase that, in addition to its well-
known role in hemostasis, has a crucial role in angiogenesis, maintenance of pregnancy …

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

ABSTRACT Background: Rare bleeding disorders (RBDs) are heterogeneous disorders,
mostly inherited in an autosomal recessive pattern. Iran is a Mideast country with a high rate …

Intracranial hemorrhage (ICH), as a life-threatening bleeding among all kinds of congenital
bleeding disorders (CBDs), is a rare manifestation except in factor XIII (FXIII) deficiency …

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 …

Background: Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with
estimated incidence of one per two million. All routine coagulation tests are normal in FXIII …

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 …

Factor XIII Deficiency - StatPearls - NCBI Bookshelf US flag An official website of the United
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Rare coagulation disorders (RCDs) are a group of diseases due to coagulation factors
deficiency leading to life-long bleeding diathesis. The diagnosis of RCDs is challenging due …

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 …