Late Diagnosis of Primary Hyperoxaluria in an Adult Patient With End-Stage Renal Disease and Bicytopenia

Primary hyperoxaluria (PH) is a rare genetic condition that disrupts the normal process of glyoxylate metabolism, resulting in an overproduction of oxalate. This excessive oxalate production leads to the accumulation of calcium oxalate (known as oxalosis) throughout various organs in the body. The u...

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Detalles Bibliográficos
Autores principales: Miry, Achref, Tbouda, Mohammed, Bouhajeb, Youssef, Abbaoui, Sanae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Pathology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450360/
https://www.ncbi.nlm.nih.gov/pubmed/37637636
http://dx.doi.org/10.7759/cureus.42469

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450360/
https://www.ncbi.nlm.nih.gov/pubmed/37637636
http://dx.doi.org/10.7759/cureus.42469

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