| Literature DB >> 32799327 |
Farrah Islam1, Stephanie Htun2, Li-Wen Lai3, Max Krall2, Menitha Poranki2, Pierre-Marie Martin4, Nara Sobreira5, Elizabeth S Wohler5, Jingwei Yu6, Anthony T Moore7, Anne M Slavotinek2.
Abstract
Next-generation sequencing strategies have resulted in mutation detection rates of 21% to 61% in small cohorts of patients with microphthalmia, anophthalmia and coloboma (MAC), but despite progress in identifying novel causative genes, many patients remain without a genetic diagnosis. We studied a cohort of 19 patients with MAC who were ascertained from a population with high rates of consanguinity. Using single nucleotide polymorphism (SNP) arrays and whole exome sequencing (WES), we identified one pathogenic variant in TENM3 in a patient with cataracts in addition to MAC. We also detected novel variants of unknown significance in genes that have previously been associated with MAC, including KIF26B, MICU1 and CDON, and identified variants in candidate genes for MAC from the Wnt signaling pathway, comprising LRP6, WNT2B and IQGAP1, but our findings do not prove causality. Plausible variants were not found for many of the cases, indicating that our current understanding of the pathogenesis of MAC, a highly heterogeneous group of ocular defects, remains incomplete.Entities:
Keywords: Anophthalmia; CDON; Coloboma; Microphthalmia; TENM3; cataract
Year: 2020 PMID: 32799327 PMCID: PMC8077035 DOI: 10.1111/cge.13830
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438