Patients with SERPINC1 rs2227589 polymorphism found to have multiple cerebral venous sinus thromboses despite a normal antithrombin level: A case report

BACKGROUND: The hereditary antithrombin (AT) deficiency caused by SERPINC1 gene mutation is an autosomal dominant thrombotic disorder. An increasing number of studies have shown that mutations in the SERPINC1 rs2227589 polymorphic site are correlated with a risk of venous thromboembolism (VTE) at co...

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Detalles Bibliográficos
Autores principales: Liao, Feng, Zeng, Jun-Ling, Pan, Jian-Gang, Ma, Jing, Zhang, Zhi-Jian, Lin, Zhi-Jun, Lin, Li-Feng, Chen, Yu-Sen, Ma, Xiao-Tang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771368/
https://www.ncbi.nlm.nih.gov/pubmed/35097087
http://dx.doi.org/10.12998/wjcc.v10.i2.618

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771368/
https://www.ncbi.nlm.nih.gov/pubmed/35097087
http://dx.doi.org/10.12998/wjcc.v10.i2.618

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