Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic

BACKGROUND: One of the most common rare inherited bleeding disorders, congenital factor VII (FVII) deficiency typically has a milder bleeding phenotype than other rare bleeding disorders. Categorizing severity in terms of factor activity associated with hemophilia (severe <1%, moderate 1%–5%, mil...

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Detalles Bibliográficos
Autores principales: Jain, Shilpa, Donkin, Jennifer, Frey, Mary-Jane, Peltier, Skye, Gunawardena, Sriya, Cooper, David L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250109/
https://www.ncbi.nlm.nih.gov/pubmed/30510462
http://dx.doi.org/10.2147/JBM.S157633

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250109/
https://www.ncbi.nlm.nih.gov/pubmed/30510462
http://dx.doi.org/10.2147/JBM.S157633

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