Mowat-Wilson syndrome (MWS) is a disorder caused by mutations or deletions of the zinc finger E-box-binding homeobox 2 (ZEB2) gene. Diagnosis of MWS can be challenging to neurologists, because its manifestations are diverse and the spectrum of genetic mutations are broad. Here, we describe two patients with MWS who initially showed atypical forms of fever-triggered seizures during childhood. Both had characteristic facial features, cognitive impairment, and genito-urinary anomalies consistent with MWS. By performing targeted next-generation sequencing (NGS) using a gene panel for epilepsy, we were able to identify a nonsense mutation (c.1965C>A) in the ZEB2 gene of one patient and a frameshift mutation (c.2348dupC) in the other patient. Fev...
Mowat–Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation ...
Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with m...
Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with m...
MowatWilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of the...
Mowat-Wilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of th...
Objective To present a seven-cases serie of Mowat-Wilson syndrome (MWS). ...
Mowat-Wilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of th...
Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly-mental retardation complex caused by mu...
Mowat-Wilson syndrome (MWS) is a rare genetic disorder that causes systemic deficiencies and abnorma...
Mowat-Wilson syndrome (MWS) is characterized by severe mental retardation with seizures, specific fa...
Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by distinctive facia...
Mowat–Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial features, moder...
Mowat-Wilson syndrome (MWS) is a rare genetic condition where variable and multiple congenital anoma...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
PurposeMowat-Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies s...
Mowat–Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation ...
Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with m...
Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with m...
MowatWilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of the...
Mowat-Wilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of th...
Objective To present a seven-cases serie of Mowat-Wilson syndrome (MWS). ...
Mowat-Wilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of th...
Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly-mental retardation complex caused by mu...
Mowat-Wilson syndrome (MWS) is a rare genetic disorder that causes systemic deficiencies and abnorma...
Mowat-Wilson syndrome (MWS) is characterized by severe mental retardation with seizures, specific fa...
Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by distinctive facia...
Mowat–Wilson syndrome (MWS) is a genetic disease characterized by distinctive facial features, moder...
Mowat-Wilson syndrome (MWS) is a rare genetic condition where variable and multiple congenital anoma...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
PurposeMowat-Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies s...
Mowat–Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation ...
Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with m...
Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with m...