Mowat-Wilson syndrome: the first two Malaysian cases

Mowat-Wilson syndrome (MWS) is a recently delineated mental retardation; a multiple congenital anomaly syndrome characterised by a typical facial gestalt, Hirschsprung disease or severe constipation, genitourinary anomaly, congenital heart defects, agenesis of corpus callosum and eye defects. Some c...

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Veröffentlicht in:	Singapore medical journal 2010-03, Vol.51 (3), p.e54-e57
Hauptverfasser:	Balasubramaniam, S, Keng, W T, Ngu, L H, Michel, L G, Irina, G
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - diagnosis Abnormalities, Multiple - genetics Child Child, Preschool Constipation Epilepsy - genetics Female Gene Deletion Hirschsprung Disease - genetics Homeodomain Proteins - genetics Humans Malaysia Repressor Proteins - genetics Zinc Finger E-box Binding Homeobox 2
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