Presentation
Variable presentations of rare genetic renal interstitial diseases. Clin J Am Soc Nephrol. 2014;9:437-9. [ Links ] 11. Eckardt K-U, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, et al. [scielo.isciii.es]
Entire Body System
- Anemia
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure. Am J Hum Genet. 2009;85:204-13. [ Links ] 18. Kemter E, Krebs S, Wanke R. [scielo.isciii.es]
Urogenital
- Kidney Failure
Kidney Int. 2011;80:768-76. [ Links ] 17. Zivná M, Hulková H, Matignon M, Hodanová K, Vylet'al P, Kalbácová M, et al. Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure. [scielo.isciii.es]
Workup
Serum
- Hyperuricemia
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure. Am J Hum Genet. 2009;85:204-13. [ Links ] 18. Kemter E, Krebs S, Wanke R. [scielo.isciii.es]
Treatment
Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone. Clin Nephrol. 2010;74:411-22. [ Links ] 40. Kmoch S, Živná M, Bleyer AJ. [scielo.isciii.es]
Prognosis
Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood. Kidney Int. 2011;80:768-76. [ Links ] 17. Zivná M, Hulková H, Matignon M, Hodanová K, Vylet'al P, Kalbácová M, et al. [scielo.isciii.es]