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Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35.

Authors :
Xiaodong Jiao
Munier, Francis L.
Schorderet, Daniel F.
Zografos, Leonidas
Smith, Janine
Rubin, Benjamin
Hejtmancik, J. Fielding
Source :
Human Genetics; May2003, Vol. 112 Issue 5/6, p593-599, 7p
Publication Year :
2003

Abstract

Francois-Neetens fleck (mouchetée) corneal dystrophy is an autosomal dominant corneal dystrophy characterized by scattered small white flecks occurring at all levels of the corneal stroma. We report linkage of the CFD locus to D2S2289 (Z<subscript>max</subscript>=4.46, θ=0), D2S325 (Z<subscript>max</subscript>=3.28, θ=0), D2S317 (Z<subscript>max</subscript>=3.1, θ=0), D2S143 (Z<subscript>max</subscript>=3.8, θ=0.03), and D2S2382 (Z<subscript>max</subscript>=5.0, θ=0) on chromosome 2q35. Multipoint analysis confirmed linkage to the region between D2S117 and D2S126 with a maximum multipoint lod score of 5.0 located midway between D2S2289 and D2S325. Analysis of CFD in these same families assuming a 90% penetrance increased the maximum lod score to 6.28 at D2S157. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03406717
Volume :
112
Issue :
5/6
Database :
Complementary Index
Journal :
Human Genetics
Publication Type :
Academic Journal
Accession number :
16115541
Full Text :
https://doi.org/10.1007/s00439-002-0905-1