लोड हो रहा है...
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...
में बचाया:
| में प्रकाशित: | Clin Med Insights Arthritis Musculoskelet Disord |
|---|---|
| मुख्य लेखकों: | , , |
| 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 |
| टैग : |
टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
|