Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management.
Elif ArıkÖzlem KeskinSerpil AlbayrakMehmet KeskinMahmut CesurMurat KaraoglanGaye InalAhmet YildirimErcan KucukosmanogluPublished in: Journal of pediatric endocrinology & metabolism : JPEM (2024)
HSR may develop during enzyme replacement therapy, which are vital in lysosomal storage diseases, and discontinuation of enzyme replacement therapy is a significant loss for patients with metabolic disorders. These reactions can be treated with premedication and long-term infusions, but some patients may require desensitization protocols for continued treatment.