Hereditary factor XII deficiency in an adult patient: A case report

Factor XII deficiency is a rare autosomal recessive health condition usually discovered incidentally during routine coagulation screening before surgery after investigating a prolongation of the activated partial thromboplastin time. This is a case of a 29-year-old man from Saudi Arabia who was sele...

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Detalles Bibliográficos
Autores principales: Al-Ansari, Rehab Y, Al-Yami, Fatimah, Almulhim, Ghayah, Woodman, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393349/
https://www.ncbi.nlm.nih.gov/pubmed/36003888
http://dx.doi.org/10.1177/2050313X221118728

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393349/
https://www.ncbi.nlm.nih.gov/pubmed/36003888
http://dx.doi.org/10.1177/2050313X221118728

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