Case Report
Mowat-Wilson Syndrome: The First Clinical and Molecular Report of an Indonesian Patient
Table 1
Clinical features of our patient compared to those in published cases of MWS with proven ZEB2 mutations.
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*Adapted from Garavelli and Mainardi (2007) [4]. **Symptoms not observed although the gold standard diagnosis has not been performed. NT: Not Tested, HSCR: Hirschprung Disease, CHD: Congenital Heart Defect, CCA: Corpus Callosum. |