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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Detalles Bibliográficos
Autores principales: Shen, Guohua, Zhang, Yuwei, Hu, Shuang, Liu, Bin, Kuang, Anren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380280/
https://www.ncbi.nlm.nih.gov/pubmed/28353596
http://dx.doi.org/10.1097/MD.0000000000006493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380280/
https://www.ncbi.nlm.nih.gov/pubmed/28353596
http://dx.doi.org/10.1097/MD.0000000000006493

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