“…Unlike other forms of renal osteodystrophy, the osteomalacia/rickets of dRTA is clearly dependent on the presence of acidosis, for it does not occur in patients in whom acidosis is prevented by alkali treatment, or in those with the incomplete syndrome of dRTA in whom the acidification defect is not sufficiently severe to cause acidosis, and when present it can be healed by correction of acidosis with alkali. Furthermore osteomalacia can complicate the very similar hyperchloraemic acidosis of uretero-colic anastomosis, where the kidneys are not diseased, and here, as in dRTA, the bone disease heals when acidosis is corrected by alkali treatment [15, 16]. Paradoxically osteomalacia/rickets has not been reported in many hereditary forms of chronic metabolic acidosis, such as methyl-malonic and propionic acidaemias, in which acidosis is present from birth and usually even more severe than in dRTA.…”