open79siPurposeMowat-Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies syndrome caused by heterozygous mutation of the ZEB2 gene. It is generally underestimated because its rarity and phenotypic variability sometimes make it difficult to recognize. Here, we aimed to better delineate the phenotype, natural history, and genotype-phenotype correlations of MWS.MethodsIn a collaborative study, we analyzed clinical data for 87 patients with molecularly confirmed diagnosis. We described the prevalence of all clinical aspects, including attainment of neurodevelopmental milestones, and compared the data with the various types of underlying ZEB2 pathogenic variations.ResultsAll anthropometric, somatic, and behavior...
Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or...
Mowat–Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial features, moder...
Mowat-Wilson syndrome (MWS) is a rare genetic disorder that causes systemic deficiencies and abnorma...
Mowat-Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies syndrome...
Purpose: Mowat–Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies...
Purpose: Mowat–Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies...
none58siPurpose:Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial...
Mowat-Wilson Syndrome (MWS) (OMIM # 235730) is a rare disorder due to ZEB2 gene defects (heterozygou...
Purpose: Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial featur...
Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or...
Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or...
Mowat–Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial features, moder...
Mowat-Wilson syndrome (MWS) is a rare genetic disorder that causes systemic deficiencies and abnorma...
Mowat-Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies syndrome...
Purpose: Mowat–Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies...
Purpose: Mowat–Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies...
none58siPurpose:Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial...
Mowat-Wilson Syndrome (MWS) (OMIM # 235730) is a rare disorder due to ZEB2 gene defects (heterozygou...
Purpose: Mowat-Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial featur...
Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or...
Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or...
Mowat–Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial features, moder...
Mowat-Wilson syndrome (MWS) is a rare genetic disorder that causes systemic deficiencies and abnorma...