Hypercoagulability and Inflammatory Markers in a Case of Congenital Thrombotic Thrombocytopenic Purpura Complicated by Fetal Demise

Background: Congenital thrombotic thrombocytopenic purpura (cTTP) is a rare disorder caused by an inherited genetic deficiency of ADAMTS13 and affects less than one per million individuals. Patients who are diagnosed with TTP during pregnancy are at increased risk of maternal and fetal complications...

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Detalles Bibliográficos
Autores principales: Skeith, Leslie, Hurd, Kelle, Chaturvedi, Shruti, Chow, Lorraine, Nicholas, Joshua, Lee, Adrienne, Young, Daniel, Goodyear, Dawn, Soucie, Jennifer, Girard, Louis, Dufour, Antoine, Agbani, Ejaife O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737388/
https://www.ncbi.nlm.nih.gov/pubmed/36498688
http://dx.doi.org/10.3390/jcm11237115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737388/
https://www.ncbi.nlm.nih.gov/pubmed/36498688
http://dx.doi.org/10.3390/jcm11237115

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