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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Clin Med Insights Arthritis Musculoskelet Disord
मुख्य लेखकों: Rathore, Farooq A., Ayaz, Saeed B., Mansoor, Sahibzada N.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Libertas Academica 2016
विषय:
ऑनलाइन पहुंच: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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