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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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| Yayımlandı: | NDT Plus |
|---|---|
| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2009
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| Konular: | |
| Online Erişim: | 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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