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Cerebro-spinal and renal ochronosis: A rare case report
Alkaptonuria, a rare inborn error of tyrosine metabolism, characterized by the absence of homogentisic acid oxidase results in the accumulation of homogentisic acid in the body. Associated renal failure and cerebral infarction is rare and usually occurs in the later stages of the disease. We report...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3453108/ https://ncbi.nlm.nih.gov/pubmed/23105912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12291-010-0038-6 |
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