| Literature DB >> 1980096 |
M Schwartz1, M Haim, D Skarsholm.
Abstract
Linkage analysis in a family with X-linked myopia gave a positive LOD score (z = 4.8 at theta = 0) for linkage to F8C. These results suggest a provisional assignment for the locus of this syndrome to the distal part of the X chromosome at Xq28. Based on the clinical and genetic evidence, a redefinition of this clinical syndrome, named Bornholm Eye Disease (BED), was made to include amblyopia, myopia, and deuteranopia. Facultative signs were optic nerve hypoplasia, reduced electroretinographic flicker function, and non-specific retinal pigment abnormalities.Entities:
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Year: 1990 PMID: 1980096
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438