DOI QR코드

DOI QR Code

Congenital nephrogenic diabetes insipidus with end-stage renal disease

  • Ryu, Hyun Ho (Department of Emergency Medicine, Chonnam National University Hospital) ;
  • Chung, Jong Hoon (Division of Nephrology, Department of Internal Medicine, Chosun University School of Medicine) ;
  • Shin, Byung Chul (Division of Nephrology, Department of Internal Medicine, Chosun University School of Medicine) ;
  • Kim, Hyun Lee (Division of Nephrology, Department of Internal Medicine, Chosun University School of Medicine)
  • Received : 2009.01.15
  • Accepted : 2009.09.18
  • Published : 2015.03.01

Abstract

Keywords

References

  1. Weller CG, Elliott W, Gusman AR. Hereditary diabetes insipidus: unusual urinary tract changes. J Urol 1950;64:716-721. https://doi.org/10.1016/S0022-5347(17)68700-7
  2. Deen PM, Marr N, Kamsteeg EJ, van Balkom BW. Nephrogenic diabetes insipidus. Curr Opin Nephrol Hypertens 2000;9:591-595. https://doi.org/10.1097/00041552-200011000-00001
  3. Cheong HI, Park HW, Ha IS, et al. Six novel mutations in the vasopressin V2 receptor gene causing nephrogenic diabetes insipidus. Nephron 1997;75:431-437. https://doi.org/10.1159/000189581
  4. Seu BW, Kim KS. A case of nephrogenic diabetes insipidus associated with urinary incontinence. Korean J Urol 1991;32:825-828.
  5. Kim HE, Han HS, Kim BC, et al. A case of autosomal dominant nephrogenic diabetes insipidus with renal failure. Korean J Nephrol 2004;23:965-969.

Cited by

  1. From infancy to adulthood: challenges in congenital nephrogenic diabetes insipidus vol.33, pp.8, 2015, https://doi.org/10.1515/jpem-2019-0529