Autoimmune Heparin-Induced Thrombocytopenia

Autoimmune thrombocytopenia (aHIT) is a severe subtype of heparin-induced thrombocytopenia (HIT) with atypical clinical features caused by highly pathological IgG antibodies (“aHIT antibodies”) that activate platelets even in the absence of heparin. The clinical features of aHIT include: the onset o...

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Detalles Bibliográficos
Autor principal: Warkentin, Theodore E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649402/
https://www.ncbi.nlm.nih.gov/pubmed/37959386
http://dx.doi.org/10.3390/jcm12216921

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649402/
https://www.ncbi.nlm.nih.gov/pubmed/37959386
http://dx.doi.org/10.3390/jcm12216921

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