Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen...

deposition of fibrinogen in the liver, kidneys, and other tissues. Congenital afibrinogenemia is a rare and generally autosomal recessive inherited disorder...

fibrinogen disorders: afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and hypodysfibrinogenemia. Congenital afibrinogenemia is defined as a lack...

depositions to develop into clots. Congenital hypofibrinogenemia must be distinguished from: a) congenital afibrinogenemia, a rare disorder in which blood...

Hypoprothrombinemia/II Factor VII deficiency Factor X deficiency Factor XII deficiency Factor XIII deficiency Dysfibrinogenemia Congenital afibrinogenemia...

Bernard–Soulier syndrome Von Willebrand disease Vitamin K deficiency Congenital afibrinogenemia Coagulopathy "Hemophilia C: Practice Essentials, Etiology, Epidemiology"...

Prolonged Decreased Uremia Unaffected Unaffected Prolonged Unaffected Congenital afibrinogenemia Prolonged Prolonged Prolonged Unaffected Factor V deficiency Prolonged...

kidneys, or other organs and tissues. These disorders include: Congenital afibrinogenemia, an inherited blood disorder in which blood does not clot normally...

Prolonged Decreased Uremia Unaffected Unaffected Prolonged Unaffected Congenital afibrinogenemia Prolonged Prolonged Prolonged Unaffected Factor V deficiency Prolonged...

nature of the defect. Platelet disorders are either congenital or acquired. Examples of congenital platelet disorders are Glanzmann's thrombasthenia, Bernard–Soulier...