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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Serbian Medical Society
2009-01-01
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Series: | Srpski Arhiv za Celokupno Lekarstvo |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0370-8179/2009/0370-81790908426C.pdf |