Hyperfibrinolysis secondary to acquired factor XIII deficiency A case report

Hyperfibrinolysis induced by factor XIII deficiency (FXIIID) is extremely rare, and patients with no manifestations of active bleeding can easily and frequently be neglected in clinical practice, leading to a missed diagnosis. Herein, we report a rare case of idiopathic FXIIID with secondary hyperfi...

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Detalles Bibliográficos
Autores principales: Gao, Lingsu, Li, Dengju, Ding, Meiqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302284/
https://www.ncbi.nlm.nih.gov/pubmed/35866832
http://dx.doi.org/10.1097/MD.0000000000029446

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302284/
https://www.ncbi.nlm.nih.gov/pubmed/35866832
http://dx.doi.org/10.1097/MD.0000000000029446

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