Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management

Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management

Congenital fibrinogen disorders are rare pathologies of the hemostasis, comprising quantitative (afibrinogenemia, hypofibrinogenemia) and qualitative (dysfibrinogenemia and hypodysfibrinogenemia) disorders. The clinical phenotype is highly heterogeneous, being associated with bleeding, thrombosis, o...

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Auteurs principaux: Tomas Simurda, Rosanna Asselta, Jana Zolkova, Monika Brunclikova, Miroslava Dobrotova, Zuzana Kolkova, Dusan Loderer, Ingrid Skornova, Jan Hudecek, Zora Lasabova, Jan Stasko, Peter Kubisz
Format: article
Langue:EN
Publié: MDPI AG 2021
Sujets:
afibrinogenemia
hypofibrinogenemia
genetic testing
global coagulation assays
bleeding
thrombosis
Medicine (General)
R5-920
Accès en ligne:https://doaj.org/article/1b2962a9071f4dddb96c55543b50554b
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https://doaj.org/article/1b2962a9071f4dddb96c55543b50554b

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