Case Report: Unmasked Inherited Dysfibrinogenemia After Everolimus Therapy

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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Bibliographic Details
Main Authors: Alona A. Merkulova, Steven C. Mitchell, Sergei Merkulov, Alisa S. Wolberg, Marguerite Neerman-Arbez, Alvin H. Schmaier
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Medicine
Subjects:
dysfibrinogenemia
everolimus
CVID
fibrin polymerization
dysfibrinogenemia Krakow III
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2020.591546/full

Internet

https://www.frontiersin.org/articles/10.3389/fmed.2020.591546/full

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