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Cystinuria in a patient with polycystic kidney disease

Cystinuria is a rare autosomal recessive metabolic disorder of renal and intestinal cystine transport. Cystine stones are found in only 1–2% of all stone formers. Patients with cystinuria are at high risk for nephrolithiasis and subsequent morbidity. Our patient is a 37-year-old male who presented f...

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Publicado en:NDT Plus
Autores principales: Love, Kate, Yeo, Fred E.
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2009
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4421477/
https://ncbi.nlm.nih.gov/pubmed/25949280
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndtplus/sfn166
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