Clinical Case Reports (Apr 2021)

Transition to lanadelumab‐flyo from three medications for a hereditary angioedema patient with a variant in the SYTL2 gene: A case report

  • Stephanie Burns,
  • Elena Lewis

DOI
https://doi.org/10.1002/ccr3.4060
Journal volume & issue
Vol. 9, no. 4
pp. 2438 – 2441

Abstract

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Abstract Non‐SERPING1 gene variant hereditary angioedema patients often need to take progesterone, attenuated androgens, and antifibrinolytics to control symptoms. These drugs may need to be tapered to extinction or reduced as lanadelumab‐flyo reaches maximum concentration.

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