Primary Hyperoxaluria Type 1 Disease Manifestations and Healthcare Utilization: A Multi-Country, Online, Chart Review Study

Background: Primary hyperoxaluria type 1 (PH1) is a rare genetic disease that can result in irreversible damage to the kidneys and, eventually, extrarenal organs. While kidney failure is a known consequence of PH1, few studies to date have characterized clinical consequences of PH1 prior to kidney f...

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Detalles Bibliográficos
Autores principales: Wang, Xiangling, Danese, David, Brown, Thomas, Baldwin, Jessica, Sajeev, Gautam, Cook, Erin E., Wang, Yao, Xu, Chunyi, Yang, Hongbo, Moritz, Michael L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488346/
https://www.ncbi.nlm.nih.gov/pubmed/34616753
http://dx.doi.org/10.3389/fmed.2021.703305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488346/
https://www.ncbi.nlm.nih.gov/pubmed/34616753
http://dx.doi.org/10.3389/fmed.2021.703305

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