Literature DB >> 12657606

An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.

Michel Michaelides1, Samantha Johnson, Arabella Poulson, Keith Bradshaw, Caren Bellmann, David M Hunt, Anthony T Moore.   

Abstract

PURPOSE: To describe the phenotype of an autosomal dominant macular dystrophy and identify the chromosomal locus.
METHODS: Eleven members of a five-generation, nonconsanguineous British family were examined clinically and also underwent automated perimetry, electrodiagnostic testing, fundus fluorescein angiography, and fundus autofluorescence imaging. Blood samples were taken for DNA extraction and linkage analysis was performed.
RESULTS: The phenotype is characterized by bull's-eye macular dystrophy first evident in the first or second decade of life. There is mild visual impairment, central scotomata, and electrophysiological testing indicates that most affected individuals have disease confined to the central retina but older subjects have more widespread rod and cone abnormalities, demonstrated by flash ERG. Genetic linkage analysis established linkage to chromosome 4 at p15.2-16.3 with a maximum lod score of 3.03 at a recombination fraction of 0.00 for marker D4S391. The locus for this autosomal dominant macular dystrophy lies between flanking markers D4S3023 and D4S3022, and overlaps the Stargardt 4 locus.
CONCLUSIONS: A new locus was identified for a bull's-eye macular dystrophy on the short arm of chromosome 4.

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Year:  2003        PMID: 12657606     DOI: 10.1167/iovs.02-0941

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  19 in total

1.  Defining the human macula transcriptome and candidate retinal disease genes using EyeSAGE.

Authors:  Catherine Bowes Rickman; Jessica N Ebright; Zachary J Zavodni; Ling Yu; Tianyuan Wang; Stephen P Daiger; Graeme Wistow; Kathy Boon; Michael A Hauser
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-06       Impact factor: 4.799

Review 2.  Protein misfolding and retinal degeneration.

Authors:  Radouil Tzekov; Linda Stein; Shalesh Kaushal
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-11-01       Impact factor: 10.005

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Authors:  Z Yang; G Kitsos; Z Tong; M Payne; S Gorezis; K Psilas; M Grigoriadou; Y Zhao; S Kamaya; G Aperis; M B Petersen; K Zhang
Journal:  J Med Genet       Date:  2006-12       Impact factor: 6.318

4.  The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy.

Authors:  Michel Michaelides; Marie-Claire Gaillard; Pascal Escher; Leila Tiab; Matthew Bedell; François-Xavier Borruat; Daniel Barthelmes; Ruben Carmona; Kang Zhang; Edward White; Michelle McClements; Anthony G Robson; Graham E Holder; Keith Bradshaw; David M Hunt; Andrew R Webster; Anthony T Moore; Daniel F Schorderet; Francis L Munier
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-04-14       Impact factor: 4.799

5.  Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy.

Authors:  Francesca I Arrigoni; Mar Matarin; Pamela J Thompson; Michel Michaelides; Michelle E McClements; Elizabeth Redmond; Lindsey Clarke; Elizabeth Ellins; Saifullah Mohamed; Ian Pavord; Nigel Klein; David M Hunt; Anthony T Moore; Julian Halcox; Sanjay M Sisodiya
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6.  ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy.

Authors:  M Michaelides; L L Chen; M A Brantley; J L Andorf; E M Isaak; S A Jenkins; G E Holder; A C Bird; E M Stone; A R Webster
Journal:  Br J Ophthalmol       Date:  2007-12       Impact factor: 4.638

Review 7.  The genetics of inherited macular dystrophies.

Authors:  M Michaelides; D M Hunt; A T Moore
Journal:  J Med Genet       Date:  2003-09       Impact factor: 6.318

8.  Quantitative fundus autofluorescence distinguishes ABCA4-associated and non-ABCA4-associated bull's-eye maculopathy.

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9.  Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.

Authors:  Zhenglin Yang; Yali Chen; Concepcion Lillo; Jeremy Chien; Zhengya Yu; Michel Michaelides; Martin Klein; Kim A Howes; Yang Li; Yuuki Kaminoh; Haoyu Chen; Chao Zhao; Yuhong Chen; Youssef Tawfik Al-Sheikh; Goutam Karan; Denis Corbeil; Pascal Escher; Shin Kamaya; Chunmei Li; Samantha Johnson; Jeanne M Frederick; Yu Zhao; Changguan Wang; D Joshua Cameron; Wieland B Huttner; Daniel F Schorderet; Frances L Munier; Anthony T Moore; David G Birch; Wolfgang Baehr; David M Hunt; David S Williams; Kang Zhang
Journal:  J Clin Invest       Date:  2008-08       Impact factor: 14.808

10.  Cone-rod dystrophy and a frameshift mutation in the PROM1 gene.

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Journal:  Mol Vis       Date:  2009-08-28       Impact factor: 2.367

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