Immunological studies on factor X antigen in patients with congenital factor X deficiency.
نویسندگان
چکیده
منابع مشابه
Recurrent Venous Thromboembolic Events in a Child with Severe Factor X Deficiency
Congenital factor X deficiency is a rare autosomal recessive bleeding disorder that presents with variable bleeding tendency and prolonged coagulation tests, prothrombin time, and partial thromboplastin time. Thromboembolic events have not been reported in patients with factor X deficiency yet. Herein, we report a patient with factor X deficiency who had recurrent venous thromboembolic events.
متن کاملPhenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency.
Factor X deficiency is a severe rare hemorrhagic condition inherited as an autosomal recessive trait. It is one of the most severe recessive inherited coagulation disorders. We analyzed the clinical manifestations, laboratory phenotype and genotype in 10 patients with severe Factor X deficiency and in their heterozygous relatives. The most frequent bleeding episodes were hematomas (70%) and gum...
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discussions as one ich patient whose pt and aptt suggest a coagulation disorder secondary to vitamin k deficiency or coagulation factor deficiency, unresponsiveness to vitamin k therapy should be useful to take fx deficiency into consideration. background inborn factor x deficiency (fxd) is a very rare (1: 500,000) hereditary coagulation disorder, which is characterized by clinical manifestatio...
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T congenital factor X (FX) is a plasmatic glycoprotein, which plays a crucial role in coagulation. Its deficit is among rare causes of the hemorrhage in child. It could be acquired or congenital. The main hemorrhagic manifestations are epistaxis, hematuria, and menorrhagia in females, sometimes hemarthrosis even craniocerebral hemorrhage. The measurement of the FX rate in the blood allows the d...
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Stuart Prower factor (Factor X) deficiency is a rare hereditary autosomal recessive coagulation disorder. We have come across three cases in the course of last 20 years at our institute. These patients presented with prolonged bleeding after minor trauma, epistaxis, subcutaneous bluish black nodules and two of them presented with history of consanguinity in parents. Hematological findings in co...
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ژورنال
عنوان ژورنال: Blood & Vessel
سال: 1984
ISSN: 0386-9717,1884-2372
DOI: 10.2491/jjsth1970.15.333