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
Publicado en:Front Med (Lausanne)
Main Authors: 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: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2021
Assuntos:
Medicine
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8062902/
https://ncbi.nlm.nih.gov/pubmed/33898474
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmed.2021.592357
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