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Article

Sleep disturbance in Mowat-Wilson syndrome.

American journal of medical genetics. Part A - 1 Mar 2016

Evans Elizabeth, Mowat David, Wilson Meredith, Einfeld Stewart

Abstract excerpt

Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome caused by a heterozygous mutation or deletion of the ZEB2 gene. It is characterized by a distinctive facial appearance in association with intellectual disability (ID) and variable other features including agenesis of the corpus callosum, seizures, congenital heart defects, microcephaly, short stature, hypotonia, and Hirschsprung disease. The...

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Identifiers

PMID: 26686679
DOI: 10.1002/ajmg.a.37502

Genes

ZEB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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