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Article

Mowat-Wilson syndrome.

Orphanet journal of rare diseases - 24 Oct 2007

Garavelli Livia, Mainardi Paola Cerruti

Abstract excerpt

Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by a distinct facial phenotype (high forehead, frontal bossing, large eyebrows, medially flaring and sparse in the middle part, hypertelorism, deep set but large eyes, large and uplifted ear lobes, with a central depression, saddle nose with prominent rounded nasal tip, prominent columella, open mouth, with M-shaped upper lip,...

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Source

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Identifiers

PMID: 17958891
DOI: 10.1186/1750-1172-2-42
PMCID: PMC2174447

Genes

ZEB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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