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Mowat-Wilson syndrome: an underdiagnosed syndrome?

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Ullmann,  Reinhard
Molecular Cytogenetics (Reinhard Ullmann), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Zitation

Engenheiro, E., Møller, R., Pinto, M., Soares, G., Nikanorova, M., Carreira, I., et al. (2008). Mowat-Wilson syndrome: an underdiagnosed syndrome? Clinical Genetics: an International Journal of Genetics and Molecular Medicine, 73(6), 579-584. doi:10.1111/j.1399-0004.2008.00997.x.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0010-804C-3
Zusammenfassung
Mowat–Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation and variable multiple congenital abnormalities due to mutations of the ZEB2 (ZFHX1B) gene at 2q22. MWS was first described in 1998 and the causative gene was delineated in 2001. Since then, 115 different mutations of ZEB2 have been published in association with this syndrome in 161 individuals. However, recent reports suggest that due to the variability of the congenital abnormalities, this syndrome may still be underdiagnosed. We report two unrelated patients with MWS where the clinical diagnosis was established only after finding of disruption of the ZEB2 gene by a balanced translocation breakpoint and an interstitial microdeletion, respectively.