Disease | fanconi syndrome |
Phenotype | C0035579|rickets |
Sentences | 3 |
PubMedID- 20946626 | There is considerable inter- and intra-familial variability in the other manifestations of pt dysfunction, which may cause a renal fanconi syndrome with hypophosphataemic rickets, as well as in the extent of nephrocalcinosis/nephrolithiasis. |
PubMedID- 24386581 | Diagnosis of hypophosphatemic rickets due to de toni-debré-fanconi syndrome was subsequently made. |
PubMedID- 25954677 | We report a seven-year-old boy with nephropathic cystinosis who presented with all the cardinal features of renal fanconi syndrome associated with rickets, pathological fractures, stage iv chronic kidney disease (ckd) and hypothyroidism. |
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