PedAM
Pediatric Disease Annotations & Medicines
| Disease | hypokalemia |
| Phenotype | C0004775|bartter syndrome |
| Sentences | 4 |
| PubMedID- 24039833 | Ksp-osr1−/− mice exhibited a bartter syndrome-like phenotype with significant hypokalemia due to excessive renal k+ secretion and hypercalciuria. |
| PubMedID- 21626220 | Inhibition of cox-2 also reduces hyper-reninism and hypokalemia in patients with antenatal bartter syndrome. |
| PubMedID- 22282380 | The severe, steady-state hypokalemia in bartter syndrome and gitelman syndrome may abruptly become life-threatening under certain aggravating conditions. |
| PubMedID- 25619794 | bartter syndrome is associated with salt wasting, hypokalemia, metabolic alkalosis, and increased renin secretion and is caused by inactivating mutations in genes encoding ion channels and transporters that mediate salt transport in the thick ascending limb of the loop of henle [6]. |
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