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Lower urinary tract symptoms and prostatic calculi: A rare presentation of alkaptonuria
Alkaptonuria is a rare tyrosine metabolic disorder. A deficiency of homogentisic acid oxidase leads to accumulation of homogentisic acid in the body. Dark-colored urine, cutaneous pigmentations and musculoskeletal deformities are characteristic features. Storage and voiding lower urinary tract sympt...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Medknow Publications & Media Pvt Ltd
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3424908/ https://ncbi.nlm.nih.gov/pubmed/22919147 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0970-1591.98474 |
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