Literature DB >> 11296022

Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneity.

L A Donoso1, A T Frost, E M Stone, R G Weleber, I M MacDonald, G S Hageman, G W Cibis, R Ritter, A O Edwards.   

Abstract

OBJECTIVES: To characterize a disease-associated haplotype in 7 families with autosomal dominant Stargardt-like macular dystrophy and to determine whether these families share a common ancestor.
METHODS: Twenty-five polymorphic DNA markers spanning known dominant Stargardt-like gene loci were used to determine the haplotype associated with disease. In addition, an extensive genealogical investigation searching for a common ancestor shared by all of the 7 families was performed.
RESULTS: We clinically evaluated 171 patients and genotyped 145 samples. The same DNA haplotype on chromosome 6q16 was shared by all evaluated affected members within the 7 families. In addition, we were able to genealogically join all of the families into one larger family consisting of 31 branches and 2314 individuals. Twenty-seven branches have known living descendants, with 7 branches having affected family members. In addition, we refined the critical region for the gene to approximately 1000 kilobases (kb) and eliminated part or all of 9 candidate disease-causing genes.
CONCLUSIONS: Our study indicates that most reported cases of autosomal dominant Stargardt-like macular dystrophy in North America are part of a single larger family associated with a gene locus on chromosome 6q16. Furthermore, the DNA haplotype associated with disease is useful in excluding individuals with phenotypically similar retinal conditions. CLINICAL RELEVANCE: The disease-associated haplotype allows for more accurate genetic counseling to be given to individuals with a Stargardt-like phenotype inherited in an autosomal dominant pattern.

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Year:  2001        PMID: 11296022     DOI: 10.1001/archopht.119.4.564

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  9 in total

1.  Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2.

Authors:  Maurine R Hobbs; Irving B Rosen; Charles E Jackson
Journal:  Am J Hum Genet       Date:  2002-05       Impact factor: 11.025

2.  Examination of VLC-PUFA-deficient photoreceptor terminals.

Authors:  Lea D Bennett; Blake R Hopiavuori; Richard S Brush; Michael Chan; Matthew J Van Hook; Wallace B Thoreson; Robert E Anderson
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-04-24       Impact factor: 4.799

3.  A Stargardt disease-3 mutation in the mouse Elovl4 gene causes retinal deficiency of C32-C36 acyl phosphatidylcholines.

Authors:  Anne McMahon; Shelley N Jackson; Amina S Woods; Wojciech Kedzierski
Journal:  FEBS Lett       Date:  2007-11-05       Impact factor: 4.124

Review 4.  Genetics and molecular pathology of Stargardt-like macular degeneration.

Authors:  Vidyullatha Vasireddy; Paul Wong; Radha Ayyagari
Journal:  Prog Retin Eye Res       Date:  2010-01-21       Impact factor: 21.198

5.  Effect of reduced retinal VLC-PUFA on rod and cone photoreceptors.

Authors:  Lea D Bennett; Richard S Brush; Michael Chan; Todd A Lydic; Kristen Reese; Gavin E Reid; Julia V Busik; Michael H Elliott; Robert E Anderson
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-04-10       Impact factor: 4.799

6.  Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4.

Authors:  Anne McMahon; Igor A Butovich; Nathan L Mata; Martin Klein; Robert Ritter; James Richardson; David G Birch; Albert O Edwards; Wojciech Kedzierski
Journal:  Mol Vis       Date:  2007-02-26       Impact factor: 2.367

7.  Essential role of Elovl4 in very long chain fatty acid synthesis, skin permeability barrier function, and neonatal survival.

Authors:  D Joshua Cameron; Zongzhong Tong; Zhenglin Yang; Jack Kaminoh; Shin Kamiyah; Haoyu Chen; Jiexi Zeng; Yali Chen; Ling Luo; Kang Zhang
Journal:  Int J Biol Sci       Date:  2007-02-06       Impact factor: 6.580

8.  Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse.

Authors:  Christian Schori; Martin-Paul Agbaga; Richard S Brush; Radha Ayyagari; Christian Grimm; Marijana Samardzija
Journal:  PLoS One       Date:  2018-01-02       Impact factor: 3.240

Review 9.  Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

Authors:  Carla B Mellough; David H W Steel; Majlinda Lako
Journal:  Stem Cells       Date:  2009-11       Impact factor: 6.277

  9 in total

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