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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Detalles Bibliográficos
Autores principales: Simurda, Tomas, Asselta, Rosanna, Zolkova, Jana, Brunclikova, Monika, Dobrotova, Miroslava, Kolkova, Zuzana, Loderer, Dusan, Skornova, Ingrid, Hudecek, Jan, Lasabova, Zora, Stasko, Jan, Kubisz, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622093/
https://www.ncbi.nlm.nih.gov/pubmed/34829490
http://dx.doi.org/10.3390/diagnostics11112140

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622093/
https://www.ncbi.nlm.nih.gov/pubmed/34829490
http://dx.doi.org/10.3390/diagnostics11112140

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