Phenotype and renal outcomes of patients with congenital arginine vasopressin resistance
Non-obstructive hydroureteronephrosis is a common complication of congenital AVP-R. CKD frequently develops in patients with phenotypically severe congenital AVP-R, independent of AVPR2 or AQP2 mutation.
Authors
- Min‐Hua Tseng (ORCID: https://orcid.org/0000-0003-4560-9429)
- Shih‐Hua Lin (ORCID: https://orcid.org/0000-0001-6152-4885)
- Jhao-Jhuang Ding (ORCID: https://orcid.org/0000-0002-9078-2338)
- Chih-Jen Cheng
- Chih‐Chien Sung
- Jeng-Daw Tsai
Institutions
- University of Iowa (US)
- Chang Gung University (TW)
- Mackay Memorial Hospital (TW)
- Chang Gung Memorial Hospital (TW)
- National Defense Medical Center (TW)
Publication Details
- Journal
- Nephrology Dialysis Transplantation
- Published
- 2025-10-23
- DOI
- https://doi.org/10.1093/ndt/gfaf218
- Primary Topic
- Neuroendocrine regulation and behavior
- Type
- article
- Field-Weighted Citation Impact
- 0.00