Renal Fanconi with mutations in NaPi-IIa

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A renal Fanconi syndrome has been described with mutations in NaPi-IIa causing impared renal phosphate reabsorption

Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, et al. A loss-of-function mutation in NaPi-IIa and renal Fanconi’s syndrome. [Internet]. The New England journal of medicine. 2010 ;362(12):1102-9.Available from:

Philippe Campeau
Baylor College of Medicine

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