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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...
Enregistré dans:
| Publié dans: | Clin Med Insights Arthritis Musculoskelet Disord |
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| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Libertas Academica
2016
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| Sujets: | |
| Accès en ligne: | 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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