Phenotypic characterization of a WBP11-related pseudo-VATER syndome
Targeted gene/phenotype/disorder under study:WBP11 (OMIM # 619227) AbstractWBP11 (WW domain binding protein 11) plays a critical role in mRNA processing and the Notch signaling pathway. Loss-of-function WBP11 variants have previously been associated with VATER association (PMID: 33276377).We have identified a family with dominantly inherited deleterious WBP11 variation. Clinical features include complex segmentation defects, kidney hypoplasia, and prenatal cerebellar stroke.We aim to characterize the phenotypic spectrum of this dominant VATER association… Lire la suite »Phenotypic characterization of a WBP11-related pseudo-VATER syndome