Novel heterozygous F7 gene mutation (c. C1286T) associated with congenital factor VII deficiency: A case report and literature review

BACKGROUND: Congenital factor VII (FVII) deficiency is a rare inherited autosomal recessive disorder characterized by prolongation of prothrombin time and low FVII coagulation activity, which may increase the risk of bleeding. CASE PRESENTATION: A 66‐year‐old man with acute postoperative intracrania...

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Detalles Bibliográficos
Autores principales: Tang, Hua, Luan, Xingzhao, Li, Jiaqi, Jiang, Gen, Zhen, Haowen, Li, Hao, Xiang, Wei, Zhou, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102670/
https://www.ncbi.nlm.nih.gov/pubmed/35349734
http://dx.doi.org/10.1002/jcla.24349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102670/
https://www.ncbi.nlm.nih.gov/pubmed/35349734
http://dx.doi.org/10.1002/jcla.24349

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