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 […]

ZEB2 Gene Variants and Mowat-Wilson Syndrome Explained

This recent study provides a detailed review of the ZEB2 gene variants responsible for Mowat-Wilson Syndrome (MWS), highlighting their impact on protein function and interaction within the body. With a focus on the genetic mechanisms underlying MWS, the article discusses a novel variant identified in a young patient, alongside insights into how different genetic changes […]