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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Autores principales: Tomas Simurda, Rosanna Asselta, Jana Zolkova, Monika Brunclikova, Miroslava Dobrotova, Zuzana Kolkova, Dusan Loderer, Ingrid Skornova, Jan Hudecek, Zora Lasabova, Jan Stasko, Peter Kubisz
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
afibrinogenemia
hypofibrinogenemia
genetic testing
global coagulation assays
bleeding
thrombosis
Medicine (General)
R5-920
Acceso en línea:https://doaj.org/article/1b2962a9071f4dddb96c55543b50554b
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https://doaj.org/article/1b2962a9071f4dddb96c55543b50554b

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