P397: Expanding the phenotypic spectrum of DLL1-related neurodevelopmental disorder: A familial case series
Abstract
P1 underwent ventriculoperitoneal shunt placement for significant ventriculomegaly, receives ADHD therapy and school support. All siblings are followed by genetics, neurology, and developmental specialists, with therapies tailored to motor and speech delays.
Fields of Study & Subjects
Genetics and Neurodevelopmental Disorders
Fetal and Pediatric Neurological Disorders
Genomics and Rare Diseases
Publication details
- Journal / source
- Genetics in Medicine Open
- Volume
- 4
- Pages
- 103891–103891
- Publication date
- 1 January 2026
- Language
- EN