Multidisciplinary patient care in X‐linked hypophosphatemic rickets: one challenge, many perspectives

X‑linked hypophosphatemic rickets (XLH, OMIM #307800) is a rare genetic metabolic disorder caused by dysregulation of fibroblast-like growth factor 23 (FGF23) leading to profound reduction in renal phosphate reabsorption. Impaired growth, severe rickets and complex skeletal deformities are direct co...

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Detalles Bibliográficos
Autores principales: Raimann, Adalbert, Mindler, Gabriel T., Kocijan, Roland, Bekes, Katrin, Zwerina, Jochen, Haeusler, Gabriele, Ganger, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2020
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Main Topic
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098922/
https://www.ncbi.nlm.nih.gov/pubmed/31993875
http://dx.doi.org/10.1007/s10354-019-00732-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098922/
https://www.ncbi.nlm.nih.gov/pubmed/31993875
http://dx.doi.org/10.1007/s10354-019-00732-2

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