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Case Report: Unmasked Inherited Dysfibrinogenemia After Everolimus Therapy
A previously hemostatically asymptomatic patient with common variable hypogammaglobulinemia was given everolimus to prevent growth of her liver. Within several months, the patient developed a severe bleeding disorder. The bleeding was due to fibrin polymerization defect that upon sequencing was show...
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| Vydáno v: | Front Med (Lausanne) |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7729062/ https://ncbi.nlm.nih.gov/pubmed/33330551 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmed.2020.591546 |
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