A case of failure to thrive secondary to primary hyperoxaluria type 1

Primary hyperoxaluria type 1 is a rare genetic condition characterized by oxalate deposition in the kidneys. We report findings of an 8-month old female presenting with failure to thrive, poor oral intake, and kidney stones resulting in the diagnosis of primary hyperoxaluria type 1. The patient exhi...

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Detalles Bibliográficos
Autores principales: Stern, Rachel, Kuo, Vicky, Rogal, Sarah, Barron, Carly, Ahmed, Raidour, Goldwasser, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Pediatric
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413989/
https://www.ncbi.nlm.nih.gov/pubmed/32793322
http://dx.doi.org/10.1016/j.radcr.2020.07.019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413989/
https://www.ncbi.nlm.nih.gov/pubmed/32793322
http://dx.doi.org/10.1016/j.radcr.2020.07.019

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