Infantile Primary Hyperoxaluria Type 1 Treated With Lumasiran in Twin Males

Primary hyperoxaluria type 1 (PH1) is a rare genetic disease that results in oxalate overproduction leading to nephrolithiasis (NL), nephrocalcinosis (NC), kidney failure, and systemic oxalosis. Infantile PH1 is its most severe form, and it may require intensive hemodialysis followed by a liver-kidn...

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Detalles Bibliográficos
Autores principales: Aldabek, Khaled, Grossman, Oulimata K, AL-Omar, Osama, Fox, Janelle A, Moritz, Michael L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882078/
https://www.ncbi.nlm.nih.gov/pubmed/35237473
http://dx.doi.org/10.7759/cureus.21673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882078/
https://www.ncbi.nlm.nih.gov/pubmed/35237473
http://dx.doi.org/10.7759/cureus.21673

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