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This paper presents a case of Fanconi syndrome with nephrogenic diabetes insipidus, walking
inability, marked stunted growth and bony deformities in association with hypophosphatmia,
glucosuria in 5 year and 6month old boy. Aminoaciduria was confirmed by Ion exchange chro-
matographic methodCwith Model KLA-5 Auto Aminoacid analyzer). There was slight improve-
ment of symptoms due to massive Vitamin D theraphy (200,0001. U. of Calciferol monthly).
Literature... |