![Representation of ZEB2 gene exons and introns with encoded protein structure with six domains having known protein functions and multiple non-domain regions of linker polypeptides. Image provided and modified from St. Peter et al. [8] with permission.](https://mowat-wilson.org/wp-content/uploads/2025/03/Screenshot-2025-03-28-at-9.11.48 AM-1030x410.png)
ZEB2 Syndrome Variants and Clinical Outcomes
This comprehensive review examines the relationship between ZEB2 gene pathogenic variants and their impact on clinical manifestations in Mowat-Wilson Syndrome (MWS). By analyzing genetic data from individuals worldwide, the authors reveal how specific mutations influence various developmental systems, highlighting crucial insights into prognosis, care strategies, and future research directions. Dive into this detailed study to better understand the genetic underpinnings of MWS and their practical implications.
