P417: Rare case of WNK3-related neurodevelopmental disorder (Prieto syndrome): Expanding the phenotype
Abstract
The child is working with psychiatry to address behavioral concerns as well as primary care to address high BMI (most recently 32.36 kg/m2). Current medications include amantadine, buspirone, clonidine, and olanzapine. His teachers feel he is making improvements with the current IEP.
Fields of Study & Subjects
Genetics and Neurodevelopmental Disorders
Genomics and Rare Diseases
Epilepsy research and treatment
Publication details
- Journal / source
- Genetics in Medicine Open
- Volume
- 4
- Pages
- 103911–103911
- Publication date
- 1 January 2026
- Language
- EN