Five Challenging Cases of Hereditary Antithrombin Deficiency Characterized by Thrombosis or Complicated Pregnancy

Hereditary antithrombin deficiency (ATD) is a rare autosomal dominant condition (estimated prevalence 1:500–1:5000). Most ATD patients have AT activity levels 40–60% of normal. We present treatments for venous thromboembolism (VTE) in five cases of hereditary ATD. Four patients had a family history...

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Detalles Bibliográficos
Autores principales: Roberts, Jonathan C, von Drygalski, Annette, Zhou, Jenny Y, Rodgers, George M, Ansteatt, Kristin, Tarantino, Michael D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595055/
https://www.ncbi.nlm.nih.gov/pubmed/36303565
http://dx.doi.org/10.2147/JBM.S365996

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595055/
https://www.ncbi.nlm.nih.gov/pubmed/36303565
http://dx.doi.org/10.2147/JBM.S365996

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