Genetic hypophosphataemia osteomalacia regroups several rare entities, characterized by a hypophosphatemie linked to a renal phosphate wasting resulting from an excess of FGF23. These disorders begin often in the pediatric age. The late forms are very rare and their clinical expression is variable. In this regard, we report the observation of a patient with genetic hypophosphataemia osteomalacia.
Key words: Genetic hypophosphatemic osteomalacia, FGF-23, Fractures
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