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Article

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

American journal of human genetics - 1 Sept 1999

Verzijl H T, van den Helm B, Veldman B, Hamel B C, Kuyt L P, Padberg G W, Kremer H

Abstract excerpt

Möbius syndrome (MIM 157900) consists of a congenital paresis or paralysis of the VIIth (facial) cranial nerve, frequently accompanied by dysfunction of other cranial nerves. The abducens nerve is typically affected, and often, also, the hypoglossal nerve. In addition, orofacial and limb malformations, defects of the musculoskeletal system, and mental retardation are seen in patients with Möbius syndrome. Most...

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Identifiers

PMID: 10441582
DOI: 10.1086/302539
PMCID: PMC1377982

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

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