Natural History of Clinical, Laboratory, and Echocardiographic Parameters of a Primary Hyperoxaluria Cohort on Long Term Hemodialysis

Background: Primary hyperoxaluria type 1 (PH1) is a rare monogenic disorder characterized by excessive hepatic production of oxalate leading to recurrent nephrolithiasis, nephrocalcinosis, and progressive kidney damage, often requiring renal replacement therapy (RRT). Though systemic oxalate deposit...

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Detalles Bibliográficos
Autores principales: Sas, David J., Enders, Felicity T., Gunderson, Tina M., Mehta, Ramila A., Olson, Julie B., Seide, Barbara M., Banks, Carly J., Dehmel, Bastian, Pellikka, Patricia A., Lieske, John C., Milliner, Dawn S.
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/PMC8062902/
https://www.ncbi.nlm.nih.gov/pubmed/33898474
http://dx.doi.org/10.3389/fmed.2021.592357

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062902/
https://www.ncbi.nlm.nih.gov/pubmed/33898474
http://dx.doi.org/10.3389/fmed.2021.592357

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