Objectives: To present authors' experience with congenital arginine vasopressin resistance (AVP-R) in children up to 12-y-old at a tertiary care center in Northern India.
Methods: An ambispective analysis was conducted, focusing on clinical, biochemical, genetic evaluations, treatments, renal and neurological outcomes.
Results: Data from 11 patients (two females) were included, with an average delay of 18 mo between symptom onset and diagnosis.