| Literature DB >> 33806565 |
Mervyn G Thomas1, Gail D E Maconachie1,2, Helen J Kuht1, Wai-Man Chan3,4, Viral Sheth1, Michael Hisaund1, Rebecca J McLean1, Brenda Barry3,4, Bashir Al-Diri5, Frank A Proudlock1, Zhanhan Tu1, Elizabeth C Engle3,4,6,7,8, Irene Gottlob1.
Abstract
Congenital fibrosis of the extraocular muscles (CFEOM) is a congenital cranial dysinnervation disorder caused by developmental abnormalities affecting cranial nerves/nuclei innervating the extraocular muscles. Autosomal dominant CFEOM arises from heterozygous missense mutations of KIF21A or TUBB3. Although spatiotemporal expression studies have shown KIF21A and TUBB3 expression in developing retinal ganglion cells, it is unclear whether dysinnervation extends beyond the oculomotor system. We aimed to investigate whether dysinnervation extends to the visual system by performing high-resolution optical coherence tomography (OCT) scans characterizing retinal ganglion cells within the optic nerve head and retina. Sixteen patients with CFEOM were screened for mutations in KIF21A, TUBB3, and TUBB2B. Six patients had apparent optic nerve hypoplasia. OCT showed neuro-retinal rim loss. Disc diameter, rim width, rim area, and peripapillary nerve fiber layer thickness were significantly reduced in CFEOM patients compared to controls (p < 0.005). Situs inversus of retinal vessels was seen in five patients. Our study provides evidence of structural optic nerve and retinal changes in CFEOM. We show for the first time that there are widespread retinal changes beyond the retinal ganglion cells in patients with CFEOM. This study shows that the phenotype in CFEOM extends beyond the motor nerves.Entities:
Keywords: congenital cranial dysinnervation disorders; congenital fibrosis of extraocular muscles; development; optic nerve hypoplasia; optical coherence tomography; retinal ganglion cells
Mesh:
Year: 2021 PMID: 33806565 PMCID: PMC7961960 DOI: 10.3390/ijms22052575
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923