Literature DB >> 35126837

Eye manifestations in the NSUN2 intellectual disability syndrome.

Graham Pingree1, Amy Harper2,3, Jordan Snajczuk4, Natario L Couser2,4,5.   

Abstract

The NSUN2-intellectual disability syndrome is a rare disorder of the cellular transcriptome that prevents proper t-RNA splicing. This disorder interrupts cellular function and leads to an accumulation of RNA fragments, producing a constellation of symptoms including dysmorphic facies, hypotonia, microcephaly, and short stature. Eye manifestations have been reported but not well characterized. Our study presents a new case involving a 4-year-old boy with novel NSUN2 variants and clinical features consistent with the syndrome. In addition, through a systemic review, we discuss the 24 previously reported cases of the syndrome with an emphasis on the eye and ocular adnexa clinical features. IJMEG
Copyright © 2021.

Entities:  

Keywords:  5-cytosine methyltransferase; NSUN2; NSUN2 intellectual disability syndrome; NSUN2-related syndrome; t-RNA modification

Year:  2021        PMID: 35126837      PMCID: PMC8784905     

Source DB:  PubMed          Journal:  Int J Mol Epidemiol Genet        ISSN: 1948-1756


  13 in total

1.  The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population.

Authors:  Weiyi Mu; Nicoline Schiess; Jennifer L Orthmann-Murphy; Ayman W El-Hattab
Journal:  J Neurogenet       Date:  2019-02-06       Impact factor: 1.250

2.  High tRNA Transferase NSUN2 Gene Expression is Associated with Poor Prognosis in Head and Neck Squamous Carcinoma.

Authors:  Lingeng Lu; Gongjian Zhu; Hongmei Zeng; Qian Xu; Klaus Holzmann
Journal:  Cancer Invest       Date:  2018-04-21       Impact factor: 2.176

3.  Expanding the phenotype of biallelic loss-of-function variants in the NSUN2 gene: Description of four individuals with juvenile cataract, chronic nephritis, or brain anomaly as novel complications.

Authors:  Kohji Kato; Seiji Mizuno; Jenny Morton; Miho Toyama; Yuichiro Hara; Evangeline Wasmer; Alan Lehmann; Tomoo Ogi
Journal:  Am J Med Genet A       Date:  2020-10-20       Impact factor: 2.802

4.  Whole exome sequencing unravels disease-causing genes in consanguineous families in Qatar.

Authors:  S Fahiminiya; M Almuriekhi; Z Nawaz; A Staffa; P Lepage; R Ali; L Hashim; J Schwartzentruber; K Abu Khadija; S Zaineddin; H Gamal; J Majewski; T Ben-Omran
Journal:  Clin Genet       Date:  2013-10-13       Impact factor: 4.438

5.  Expression of NOL1/NOP2/sun domain (Nsun) RNA methyltransferase family genes in early mouse embryogenesis.

Authors:  Lijun Chi; Paul Delgado-Olguín
Journal:  Gene Expr Patterns       Date:  2013-06-29       Impact factor: 1.224

6.  Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.

Authors:  Muzammil Ahmad Khan; Muhammad Arshad Rafiq; Abdul Noor; Shobbir Hussain; Joana V Flores; Verena Rupp; Akshita K Vincent; Roland Malli; Ghazanfar Ali; Falak Sher Khan; Gisele E Ishak; Dan Doherty; Rosanna Weksberg; Muhammad Ayub; Christian Windpassinger; Shahnaz Ibrahim; Michaela Frye; Muhammad Ansar; John B Vincent
Journal:  Am J Hum Genet       Date:  2012-04-26       Impact factor: 11.025

7.  Histopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screen.

Authors:  Hibret A Adissu; Jeanne Estabel; David Sunter; Elizabeth Tuck; Yvette Hooks; Damian M Carragher; Kay Clarke; Natasha A Karp; Susan Newbigging; Nora Jones; Lily Morikawa; Jacqueline K White; Colin McKerlie
Journal:  Dis Model Mech       Date:  2014-03-20       Impact factor: 5.758

8.  Aberrant methylation of tRNAs links cellular stress to neuro-developmental disorders.

Authors:  Sandra Blanco; Sabine Dietmann; Joana V Flores; Shobbir Hussain; Claudia Kutter; Peter Humphreys; Margus Lukk; Patrick Lombard; Lucas Treps; Martyna Popis; Stefanie Kellner; Sabine M Hölter; Lillian Garrett; Wolfgang Wurst; Lore Becker; Thomas Klopstock; Helmut Fuchs; Valerie Gailus-Durner; Martin Hrabĕ de Angelis; Ragnhildur T Káradóttir; Mark Helm; Jernej Ule; Joseph G Gleeson; Duncan T Odom; Michaela Frye
Journal:  EMBO J       Date:  2014-07-25       Impact factor: 11.598

9.  Identification of human tRNA:m5C methyltransferase catalysing intron-dependent m5C formation in the first position of the anticodon of the pre-tRNA Leu (CAA).

Authors:  Bartosz Brzezicha; Marcin Schmidt; Izabela Makalowska; Artur Jarmolowski; Joanna Pienkowska; Zofia Szweykowska-Kulinska
Journal:  Nucleic Acids Res       Date:  2006-10-27       Impact factor: 16.971

10.  Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome.

Authors:  Fernando Jose Martinez; Jeong Ho Lee; Ji Eun Lee; Sandra Blanco; Elizabeth Nickerson; Stacey Gabriel; Michaela Frye; Lihadh Al-Gazali; Joseph G Gleeson
Journal:  J Med Genet       Date:  2012-05-10       Impact factor: 6.318

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