Young Male With End-Stage Renal Disease Due to Primary Hyperoxaluria Type 2: A Rare Presentation

Primary hyperoxaluria type 2 (PH2) is a rare genetic disorder characterized by excessive oxalate production due to glyoxylate metabolism alterations. This case report presents a 26-year-old male with PH2 who experienced recurrent nephrolithiasis since childhood, leading to end-stage renal disease (E...

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Detalles Bibliográficos
Autores principales: Kashiv, Pranjal, Dubey, Shubham, Sejpal, Kapil N, Malde, Sunny, Gurjar, Prasad, Pasari, Amit, Balwani, Manish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Nephrology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625654/
https://www.ncbi.nlm.nih.gov/pubmed/37933374
http://dx.doi.org/10.7759/cureus.46555

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625654/
https://www.ncbi.nlm.nih.gov/pubmed/37933374
http://dx.doi.org/10.7759/cureus.46555

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