Embryonal nuclear cataract (disorder)

Known as: Cataract, congenital nuclear, Cataract, embryonal nuclear, Congenital nuclear cataract 
A type of congenital cataract in which the opacities are confined to a small central area within the embryonic or fetal nuclei of the Iens. The… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1990-2018
024619902018

Papers overview

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2013
2013
Congenital cataracts are an important cause of bilateral visual impairment in infants. Through genome-wide linkage analysis in a… (More)
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2009
2009
PURPOSE To identify the genetic defect associated with autosomal dominant congenital nuclear cataract in a Chinese family… (More)
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2009
2009
PURPOSE To identify the genetic defects associated with autosomal dominant congenital nuclear cataract in a Chinese family… (More)
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2007
2007
PURPOSE Some 30% of cases of congenital cataract are genetic in origin, usually transmitted as an autosomal dominant trait. The… (More)
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2007
2007
PURPOSE To investigate a novel deletion variant of gammaD-crystallin (CRYGD) identified in a Chinese family with nuclear… (More)
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2004
2004
PURPOSE To identify the genetic defect leading to the congenital nuclear cataract affecting a large five-generation Swiss family… (More)
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2003
2003
Congenital cataracts are an important cause of blindness worldwide. In a family of Chinese descent, a dominant congenital nuclear… (More)
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2003
2003
C ataract results from a loss in transparency of the crystalline lens. Worldwide, there are an estimated 20 million people blind… (More)
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Highly Cited
1997
Highly Cited
1997
Recent reports have described families in whom a combination of elevated serum ferritin not related to iron overload and… (More)
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1995
1995
The only genetic disorder with elevated serum ferritin levels so far described is hereditary HLA-related haemochromatosis. On the… (More)
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