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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Vydáno v:Front Endocrinol (Lausanne)
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2021
Témata:
Endocrinology
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8018577/
https://ncbi.nlm.nih.gov/pubmed/33815294
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2021.641543
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