PedAM
Pediatric Disease Annotations & Medicines
| Disease | hypocalcemia |
| Phenotype | C0025362|mental retardation |
| Sentences | 1 |
| PubMedID- 20684172 | Herein, the authors summarize the progress that has been made over this period in disclosing the molecular basis of several novel gkds which were characterized in this area and include bartter syndrome type iv, type ii bartter syndrome and transient neonatal hyperkalemia, cystinuria and mental retardation, familial hypomagnesemia with secondary hypocalcemia, infantile nephronophthisis and familial hemolytic uremic syndrome with factor h deficiency. |
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