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A mimic of ankylosing spondylitis, ochronosis: case report and review of the literature
PURPOSE OF REVIEW: Ochronosis and alkaptonuria are manifestations of the same condition – a rare autosomal recessive disorder resulting from a constitutional lack of homogentisate 1,2-dioxygenase (HGD) with the consequent accumulation of homogentisic acid (HGA). In ochronosis, HGA undergoes autoxida...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285993/ https://www.ncbi.nlm.nih.gov/pubmed/33666743 http://dx.doi.org/10.1007/s11882-021-01002-1 |