Case report: A case of new mutation in SERPINC1 leading to thrombotic microangiopathy

Introduction: Hereditary antithrombin-III deficiency can significantly increase the risk for thrombosis, which is common in limb deep vein and pulmonary cases. However, thrombotic microangiopathy (TMA) caused by hereditary antithrombin deficiency is rare. Case Presentation: We reported the case of a...

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Detalles Bibliográficos
Autores principales: Li, Bing, Zhang, Xiaohui, Lv, Hailin, Yang, Xiaoqing, Gao, Yanxia, Hu, Zhao, Ma, Chengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565210/
https://www.ncbi.nlm.nih.gov/pubmed/37829283
http://dx.doi.org/10.3389/fgene.2023.1278511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565210/
https://www.ncbi.nlm.nih.gov/pubmed/37829283
http://dx.doi.org/10.3389/fgene.2023.1278511

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