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Adult-onset hypophosphatemic osteomalacia associated with Sjogren syndrome: Clinical case report
RATIONALE: Hypophosphatemic osteomalacia (HO) is a metabolic bone disease, exhibiting different etiologies such as genetic mutation, tumor induction, dysimmunity, or renal disease. Sjogren's syndrome (SS) is a connective tissue disorder commonly involving exocrine glands; however kidney involve...
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| Pubblicato in: | Medicine (Baltimore) |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wolters Kluwer Health
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5380280/ https://ncbi.nlm.nih.gov/pubmed/28353596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000006493 |
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