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Ochronotic Arthropathy: Two Case Reports from a Developing Country
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is due to the lack of an enzyme homogentisate 1,2-dioxygenase, which results in an accumulation of homogentisic acid in different areas of the body, including sclera, skin, cardiac valves, articular carti...
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| Publicado no: | Clin Med Insights Arthritis Musculoskelet Disord |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Libertas Academica
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4749042/ https://ncbi.nlm.nih.gov/pubmed/26884684 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/CMAMD.S31560 |
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