PedAM
Pediatric Disease Annotations & Medicines
| Disease | nephrocalcinosis |
| Phenotype | C0033687|proteinuria |
| Sentences | 3 |
| PubMedID- 20946626 | Dent's disease is characterized by pt dysfunction and lmw proteinuria, associated with hypercalciuria, nephrolithiasis, nephrocalcinosis, and progressive renal failure. |
| PubMedID- 23235953 | Dent's disease is an x-linked recessive proximal tubulopathy, characterized by low-molecular-weight proteinuria and hypercalciuria with nephrocalcinosis and nephrolithiasis, as well as progressive renal failure [66]. |
| PubMedID- 21859490 | Clinical characteristics of dent's disease include familial tubular syndromes such as x-linked recessive nephrolithiasis, x-linked recessive hypophosphatemic rickets and low-molecular weight proteinuria with hypercalciuria and nephrocalcinosis in japanese children [2]. |
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