Mowat-Wilson syndrome: A case report

Introduction. Mowat-Wilson syndrome (MWS) is characterised by severe mental retardation and multiple congenital anomalies. Key features for diagnosis are specific facial dysmorphism with uplifted ear lobes and Hirschsprung's disease. Ganglionic disorders of the colon, both the number of ganglio...

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Bibliographic Details
Main Authors: Čuturilo Goran, Stefanović Igor, Jovanović Ida, Miletić-Grković Slobodanka, Novaković Ivana
Format: Article
Language:English
Published: Serbian Medical Society 2009-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2009/0370-81790908426C.pdf