X-linked hypophosphatemia and growth

X-Linked hypophosphatemia (XLH) is the most common form of hereditary rickets caused by loss-of function mutations in the PHEX gene. XLH is characterized by hypophosphatemia secondary to renal phosphate wasting, inappropriately low concentrations of 1,25 dihydroxyvitamin D and high circulating level...

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Veröffentlicht in:	Reviews in endocrine & metabolic disorders 2017-03, Vol.18 (1), p.107-115
Hauptverfasser:	Fuente, R., Gil-Peña, H., Claramunt-Taberner, D., Hernández, O., Fernández-Iglesias, A., Alonso-Durán, L., Rodríguez-Rubio, E., Santos, F.
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Diabetes Endocrinology Familial Hypophosphatemic Rickets - complications Familial Hypophosphatemic Rickets - metabolism Fibroblast Growth Factors - metabolism Growth Disorders - drug therapy Growth Disorders - etiology Growth Disorders - metabolism Humans Internal Medicine Medicine Medicine & Public Health
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