Recurrent structural malformations identified among Mowat-Wilson syndrome fetuses

What's already known about this topic? Mowat–Wilson syndrome (MWS) (OMIM#235730) is a genetic disease caused by mutations or deletions of the ZEB2 gene and characterized by typical facial dysmorphism. It is rarely diagnosed prenatally. What does this study add? We report and review the ultrasou...

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Veröffentlicht in:	Prenatal diagnosis 2014-03, Vol.34 (3), p.296-298
Hauptverfasser:	Zhou, Yan, Huang, Jin, Cheng, Yvonne Kwun Yue, Leung, Tak Yeung, Pooh, Ritsuko K., Lo, Fai Man, Choy, Kwong Wai
Format:	Artikel
Sprache:	eng
Schlagworte:	Down syndrome Facies Female Fetuses Hirschsprung Disease - diagnosis Humans Intellectual Disability - diagnosis Microcephaly - diagnosis Pregnancy Prenatal Diagnosis Young Adult
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