Literature DB >> 33588793

Novel Norrie disease gene mutations in Chinese patients with familial exudative vitreoretinopathy.

Li-Yun Jia1, Kai Ma2.   

Abstract

PURPOSE: This study aims to analyze the Norrie disease gene (NDP) variants in patients with familial exudative vitreoretinopathy (FEVR) and their clinical features.
METHODS: Thirty-three Chinese patients (22 familial and 11 simplex) who were diagnosed as FEVR underwent detailed ocular examinations in Beijing Tongren Hospital. Peripheral venous blood was drawn from the patients and their family members for the extraction of genomic DNA. All exons of NDP gene were analyzed by direct sequencing of PCR-amplified DNA fragments.
RESULTS: Four novel mutations in NDP gene were identified in four X-linked FEVR families: a C → T transversion, c. 625C → T, in exon 3, resulting in a serine-to-proline change in codon 73 (S73P); a C → G transition, c. 751C → G, in exon 3, resulting in an arginine-to-glycine change in codon 115 (R115G); a T → C transversion of nucleotide 331 at 5'UTR in exon 2 (c.331 T → C); and a C → T transversion of the nucleotide 5 in intron 1 (IVS1 + 5C → T). The mutations were not present in the control group (n = 100).
CONCLUSIONS: Our results extend the spectrum of NDP gene mutations. The mutations in the non-coding region of NDP may play a crucial role in the pathogenesis of FEVR.

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Year:  2021        PMID: 33588793      PMCID: PMC7885586          DOI: 10.1186/s12886-021-01852-3

Source DB:  PubMed          Journal:  BMC Ophthalmol        ISSN: 1471-2415            Impact factor:   2.209


  25 in total

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Authors:  Johane M Robitaille; Binyou Zheng; Karin Wallace; M Jill Beis; Cuneyt Tatlidil; Jenny Yang; Tom G Sheidow; Lee Siebert; Alex V Levin; Wai-Ching Lam; Brian W Arthur; Christopher J Lyons; Elisa Jaakkola; Ekaterini Tsilou; Charles A Williams; Richard Grey Weaver; Carol L Shields; Duane L Guernsey
Journal:  Br J Ophthalmol       Date:  2010-11-21       Impact factor: 4.638

2.  Fluorescein angiographic findings in familial exudative vitreoretinopathy.

Authors:  C L Canny; G L Oliver
Journal:  Arch Ophthalmol       Date:  1976-07

3.  Novel frizzled-4 gene mutations in chinese patients with familial exudative vitreoretinopathy.

Authors:  Li-Yun Jia; Xiao-Xin Li; Wen-Zhen Yu; Wo-tan Zeng; Chen Liang
Journal:  Arch Ophthalmol       Date:  2010-10

4.  Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure.

Authors:  T Meitinger; A Meindl; P Bork; B Rost; C Sander; M Haasemann; J Murken
Journal:  Nat Genet       Date:  1993-12       Impact factor: 38.330

5.  ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature.

Authors:  Rob W J Collin; Konstantinos Nikopoulos; Margo Dona; Christian Gilissen; Alexander Hoischen; F Nienke Boonstra; James A Poulter; Hiroyuki Kondo; Wolfgang Berger; Carmel Toomes; Tomoko Tahira; Lucas R Mohn; Ellen A Blokland; Lisette Hetterschijt; Manir Ali; Johanne M Groothuismink; Lonneke Duijkers; Chris F Inglehearn; Lea Sollfrank; Tim M Strom; Eiichi Uchio; C Erik van Nouhuys; Hannie Kremer; Joris A Veltman; Erwin van Wijk; Frans P M Cremers
Journal:  Proc Natl Acad Sci U S A       Date:  2013-05-28       Impact factor: 11.205

6.  A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.

Authors:  Z Y Chen; E M Battinelli; A Fielder; S Bundey; K Sims; X O Breakefield; I W Craig
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

7.  Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

Authors:  Carmel Toomes; Helen M Bottomley; Richard M Jackson; Katherine V Towns; Sheila Scott; David A Mackey; Jamie E Craig; Li Jiang; Zhenglin Yang; Richard Trembath; Geoffrey Woodruff; Cheryl Y Gregory-Evans; Kevin Gregory-Evans; Michael J Parker; Graeme C M Black; Louise M Downey; Kang Zhang; Chris F Inglehearn
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8.  Mutation spectrum of NDP, FZD4 and TSPAN12 genes in Indian patients with retinopathy of prematurity.

Authors:  Sonika Rathi; Subhadra Jalali; Ganeswara Rao Musada; Satish Patnaik; Divya Balakrishnan; Anjli Hussain; Inderjeet Kaur
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9.  Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair.

Authors:  Qiang Xu; Yanshu Wang; Alain Dabdoub; Philip M Smallwood; John Williams; Chad Woods; Matthew W Kelley; Li Jiang; William Tasman; Kang Zhang; Jeremy Nathans
Journal:  Cell       Date:  2004-03-19       Impact factor: 41.582

10.  Structure and functional properties of Norrin mimic Wnt for signalling with Frizzled4, Lrp5/6, and proteoglycan.

Authors:  Tao-Hsin Chang; Fu-Lien Hsieh; Matthias Zebisch; Karl Harlos; Jonathan Elegheert; E Yvonne Jones
Journal:  Elife       Date:  2015-07-09       Impact factor: 8.140

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  3 in total

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Authors:  Xiaona Wang; Jun Chen; Hui Xiong; Xuhui Yu
Journal:  PLoS One       Date:  2022-07-13       Impact factor: 3.752

2.  A novel frameshift c.22_25dupGCAT mutation of the NDP gene in a Chinese infant with Norrie disease: A case report.

Authors:  He Wang; Zeyuan Liu; Yuantao Zhou; Yuanyuan Ma; Dan Tao
Journal:  Medicine (Baltimore)       Date:  2022-01-07       Impact factor: 1.889

3.  Next-generation sequencing reveals a case of Norrie disease in a child with bilateral ocular malformation.

Authors:  Haijun Li; Zhiming Li; Degang Wang; Chuanming Chen; Zhiqiang Chen; Jinhua Wang; Chenxia Xu; Xingsheng Dong
Journal:  Front Genet       Date:  2022-08-12       Impact factor: 4.772

  3 in total

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