Congenital Factor X-Riyadh (Stuart-Prower) Deficiency With Isolated Prothrombin Time Prolongation: A Case Report

Factor X (FX) deficiency is an extremely rare autosomal recessive inherited coagulation defect. We report a case of congenital Factor X-Riyadh deficiency discovered during a routine workup before a dental procedure. During routine work-up for dental surgery, prothrombin time (PT) and the internation...

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Detalles Bibliográficos
Autores principales: Alasmari, Badriah G, Tahaelbashir, Salma E, Alomari, Mohammed, Hommadi, Ashwaq M, Baothman, Abdullah, Al-tala, Saeed M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178621/
https://www.ncbi.nlm.nih.gov/pubmed/37187648
http://dx.doi.org/10.7759/cureus.37488

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178621/
https://www.ncbi.nlm.nih.gov/pubmed/37187648
http://dx.doi.org/10.7759/cureus.37488

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