Article
Mowat Wilson syndrome and Hirschsprung disease: a retrospective study on functional outcomes.
Pediatric surgery international - 1 Nov 2020
Dagorno Claire, Pio Luca, Capri Yline, Ali Liza, Giurgea Irina, Qoshe Livia, Morcrette Guillaume, Julien-Marsollier Florence, Sommet Julie, Chomton Maryline, Berrebi Dominique, Bonnard Arnaud
Abstract excerpt
AIM OF THE STUDY: Mowat Wilson syndrome (MWS) is a complex genetic disorder due to mutation or deletion of the ZEB2 gene (ZFHX1B), including multiple clinical features. Hirschsprung disease is associated with this syndrome with a prevalence between 43 and 57%. The aim of this study was to demonstrate the severe outcomes and the high complication rates in children with MWS, focusing on their complicated follow-up....
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