A Case Report on an Extremely Rare Disease: Factor XI Deficiency

Factor XI deficiency is a rare condition with an estimated prevalence of about one in one million and is more commonly seen in Ashkenazi Jews (8-9%) due to consanguinity. It occurs because of mutations in the factor XI gene (F11) on chromosome 4(4q35). Patients with this disorder may remain asymptom...

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Detalles Bibliográficos
Autores principales: Mandal, Shobha, Gami, Sumit, Shah, Surendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603878/
https://www.ncbi.nlm.nih.gov/pubmed/33150098
http://dx.doi.org/10.7759/cureus.10746

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603878/
https://www.ncbi.nlm.nih.gov/pubmed/33150098
http://dx.doi.org/10.7759/cureus.10746

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