| Literature DB >> 27181683 |
Jong G Park1, Max A Tischfield2, Alicia A Nugent3, Long Cheng4, Silvio Alessandro Di Gioia2, Wai-Man Chan5, Gail Maconachie6, Thomas M Bosley7, C Gail Summers8, David G Hunter9, Caroline D Robson10, Irene Gottlob6, Elizabeth C Engle11.
Abstract
Duane retraction syndrome (DRS) is a congenital eye-movement disorder defined by limited outward gaze and retraction of the eye on attempted inward gaze. Here, we report on three heterozygous loss-of-function MAFB mutations causing DRS and a dominant-negative MAFB mutation causing DRS and deafness. Using genotype-phenotype correlations in humans and Mafb-knockout mice, we propose a threshold model for variable loss of MAFB function. Postmortem studies of DRS have reported abducens nerve hypoplasia and aberrant innervation of the lateral rectus muscle by the oculomotor nerve. Our studies in mice now confirm this human DRS pathology. Moreover, we demonstrate that selectively disrupting abducens nerve development is sufficient to cause secondary innervation of the lateral rectus muscle by aberrant oculomotor nerve branches, which form at developmental decision regions close to target extraocular muscles. Thus, we present evidence that the primary cause of DRS is failure of the abducens nerve to fully innervate the lateral rectus muscle in early development.Entities:
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Year: 2016 PMID: 27181683 PMCID: PMC4908193 DOI: 10.1016/j.ajhg.2016.03.023
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025