Creation of an Evidence-Based Physical Therapy Program for Adults with XLH: Translational Application of an Interprofessional Clinical Study

X-linked hypophosphatemia (XLH) arises due to inactivating mutations of the PHEX gene resulting in elevated circulating levels of the hormone FGF23, producing phosphaturia and impaired intestinal phosphate absorption. XLH is a lifelong metabolic disease with musculoskeletal comorbidities that domina...

Descripción completa

Detalles Bibliográficos
Autores principales: Kanamalla, Karthik, Fuchs, Rebekah, Herzog, Casey, Steigbigel, Keith, Macica, Carolyn Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Bone and Mineral Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089516/
http://dx.doi.org/10.1210/jendso/bvab048.528

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089516/
http://dx.doi.org/10.1210/jendso/bvab048.528

Ejemplares similares