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Case Report: Sustained Efficacy of Lumasiran at 18 Months in Primary Hyperoxaluria Type 1
Background: Primary hyperoxaluria type 1 (PH1) is a rare genetic disease caused by hepatic overproduction of oxalate, ultimately responsible for kidney stones, kidney failure and systemic oxalosis. Lumasiran, is a liver-directed RNA interference therapeutic agent. It has been shown to reduce hepatic...
Autores principales: | Chiodini, Benedetta, Tram, Nathalie, Adams, Brigitte, Hennaut, Elise, Lolin, Ksenija, Ismaili, Khalid |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767018/ https://www.ncbi.nlm.nih.gov/pubmed/35071135 http://dx.doi.org/10.3389/fped.2021.791616 |
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