Primary hyperoxaluria: a case series

BACKGROUND: Primary hyperoxaluria (PH) is a rare genetic disorder characterized by the excessive production and accumulation of oxalate. We present five cases of PH, each exhibiting varying manifestations of the disorder including a case presenting as postpartum kidney failure. Notably, three of the...

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Detalles Bibliográficos
Autores principales: Rather, Jawad Iqbal, Rasheed, Rabiya, Wani, Muzafar Maqsood, Bhat, Mohammad Ashraf, Wani, Imtiyaz Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559408/
https://www.ncbi.nlm.nih.gov/pubmed/37803380
http://dx.doi.org/10.1186/s13256-023-04129-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559408/
https://www.ncbi.nlm.nih.gov/pubmed/37803380
http://dx.doi.org/10.1186/s13256-023-04129-z

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