Factor XIII deficiency in the Saudi population, an underestimated bleeding risk. Review article and an illustrative case report with dental complications

INTRODUCTION: Congenital Factor (F) XIII deficiency is an autosomal recessive disorder caused by genetic variations in either F13A or F13B genes leading to a bleeding diathesis with variable severity. Patients with severe FXIII deficiency usually present with umbilical cord bleeding during the neona...

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Detalles Bibliográficos
Autor principal: Aljabry, Mansour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213848/
https://www.ncbi.nlm.nih.gov/pubmed/37251713
http://dx.doi.org/10.1016/j.sdentj.2023.03.015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213848/
https://www.ncbi.nlm.nih.gov/pubmed/37251713
http://dx.doi.org/10.1016/j.sdentj.2023.03.015

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