Corneal endothelial dystrophy. A study of 64 families
J. H. Krachmer, J. J. Purcell Jr, C. W. Young and K. D. Bucher
A prospective study was undertaken during an 18-month period with 64
families who had endothelial dystrophy. Two hundred twenty-eight relatives
were examined. Of those older than the age of 40, 38% were affected. Women
were affected more severely and 2.5 times more frequently than men. The
disease showed a strong familial tendency: there was one family in which
three generations were affected and 16 families in which two generations
were affected. There were four families that had members with edema in two
generations. There was no association between edema in a parent and edema
in a child. The proportion of relatives affected and the severity of
involvement increased with age. Fifty-three probands and 18 relatives had
endothelial dystrophy with edema (Fuchs' dystrophy). Of these 71, one had
glaucoma.
Analysis of the Posterior Polymorphous Corneal Dystrophy 3 Gene, TCF8, in Late-Onset Fuchs Endothelial Corneal Dystrophy
Mehta et al.
IOVS 2008;49:184-188.
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British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene
Liskova et al.
Br. J. Ophthalmol. 2007;91:1717-1718.
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A Common Locus for Late-Onset Fuchs Corneal Dystrophy Maps to 18q21.2-q21.32.
Sundin et al.
IOVS 2006;47:3919-3926.
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Linkage of Late-Onset Fuchs Corneal Dystrophy to a Novel Locus at 13pTel-13q12.13
Sundin et al.
IOVS 2006;47:140-145.
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Inheritance of a Novel COL8A2 Mutation Defines a Distinct Early-Onset Subtype of Fuchs Corneal Dystrophy
Gottsch et al.
IOVS 2005;46:1934-1939.
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VSX1: A gene for posterior polymorphous dystrophy and keratoconus
Heon et al.
Hum Mol Genet 2002;11:1029-1036.
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Missense mutations in COL8A2, the gene encoding the {alpha}2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
Biswas et al.
Hum Mol Genet 2001;10:2415-2423.
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