Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium

X-linked hypophosphatemia (XLH) is the most common genetic form of hypophosphatemic rickets and osteomalacia. In this disease, mutations in the PHEX gene lead to elevated levels of the hormone fibroblast growth factor 23 (FGF23), resulting in renal phosphate wasting and impaired skeletal and dental...

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Detalles Bibliográficos
Autores principales: Laurent, Michaël R., De Schepper, Jean, Trouet, Dominique, Godefroid, Nathalie, Boros, Emese, Heinrichs, Claudine, Bravenboer, Bert, Velkeniers, Brigitte, Lammens, Johan, Harvengt, Pol, Cavalier, Etienne, Kaux, Jean-François, Lombet, Jacques, De Waele, Kathleen, Verroken, Charlotte, van Hoeck, Koenraad, Mortier, Geert R., Levtchenko, Elena, Vande Walle, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018577/
https://www.ncbi.nlm.nih.gov/pubmed/33815294
http://dx.doi.org/10.3389/fendo.2021.641543

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018577/
https://www.ncbi.nlm.nih.gov/pubmed/33815294
http://dx.doi.org/10.3389/fendo.2021.641543

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