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A Rare Sparkle: A Case of Calcified Kidneys in a Young Infant With Renal Failure
Primary hyperoxaluria-1 (PH1) is an autosomal recessively inherited rare genetic condition due to the deficiency of the hepatic enzyme alanine:glyoxylate aminotransferase which leads to high systemic levels of oxalate and subsequently, early end-stage renal disease and death. Here, we present a case...
Autores principales: | Mittal, Aliza, Jain, Hritvik, Singh, Amarpal, Yadav, Taruna, Vishwajeet, Vikarn |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636571/ https://www.ncbi.nlm.nih.gov/pubmed/37954792 http://dx.doi.org/10.7759/cureus.46827 |
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