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Article

Oculomotility Disorders Arising From Disruptions in Brainstem Motor Neuron Development

1 May 2007

Abstract excerpt

The identification and analysis of pedigrees with rare congenital oculomotility syndromes has led to the definition of the congenital cranial dysinnervation disorders. These disorders appear to result from mutations in genes that are essential to the normal development and/or connectivity of cranial motoneurons. This review highlights the clinical features and genetic etiology of 3 congenital cranial...

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Identifiers

PMID: 17502461
DOI: 10.1001/archneur.64.5.633

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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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