North Carolina macular dystrophy

Known as: NCMD, CAPED, Central areolar pigment epithelial dystrophy 
This term has been used as a general description of degeneration of the fovea. It is preferable to provide an exact phenotypic description. [HPO… (More)
National Institutes of Health

Papers overview

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2016
2016
PURPOSE To identify specific mutations causing North Carolina macular dystrophy (NCMD). DESIGN Whole-genome sequencing coupled… (More)
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2009
2009
PURPOSE To characterize the clinical phenotypes and genotype of a large family with North Carolina macular dystrophy (NCMD… (More)
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2008
2008
North Carolina macular dystrophy (NCMD) is an autosomal dominant macular disease, was mapped to 6q14-q16.2, the disease-causing… (More)
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2006
2006
PURPOSE To characterize and report the phenotype of a Korean family with an early-onset autosomal dominant macular dystrophy… (More)
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1999
1999
PURPOSE We previously reported linkage of North Carolina macular dystrophy in a single isolated family to a broad region on… (More)
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1998
1998
PURPOSE To map the gene responsible for causing a macular degeneration in a Texan family that appears clinically similar to the… (More)
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1998
1998
  • Kent W. Small
  • Transactions of the American Ophthalmological…
  • 1998
PURPOSE To study the North Carolina macular dystrophy phenotype (MCDR1) in multiple families of different ethnic backgrounds, to… (More)
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1998
1998
AIMS To document the phenotype of an autosomal dominant macular dystrophy diagnosed as having North Carolina macular dystrophy… (More)
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1998
1998
BACKGROUND Our purpose was to investigate central visual function in North Carolina macular dystrophy (MCDR1). A German family… (More)
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1992
1992
North Carolina macular dystrophy (NCMD) is an autosomal dominant macular dystrophy causing impaired central vision at an early… (More)
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