North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2.

Abstract

The macular degenerations comprise a heterogeneous group of diseases, generally reported in small families. Single, large family studies of North Carolina macular dystrophy have aided in defining the spectrum of the phenotype of this disorder and its relationship to other macular degenerations. North Carolina macular dystrophy has many phenotypic similarities to age-related macular degeneration with the glaring exception of the early age of onset of North Carolina macular dystrophy. The authors initially reported mapping this disease by linkage to the long arm of chromosome 6. They now report additional data on a total of 247 individuals in the original North Carolina macular dystrophy family whom we ascertained for clinical and molecular genetic studies. Standard clinical ophthalmic examination revealed that 96 of these individuals were affected. Molecular genetic studies increased the LOD score to 23 and refined the genomic localization of the disease-causing gene to 6q14-q16.2.

• Authors: K W Small, J Weber, A Roses, P Pericak-Vance
• Journal: Ophthalmic paediatrics and genetics (Ophthalmic Paediatr Genet) Vol. 14 Issue 4 Pg. 143-50 (Dec 1993) ISSN: 0167-6784 [Print] Netherlands
• PMID: 8015785 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S., Review)

Chemical References

• Genetic Markers

Topics

• Adult
• Aged
• Chromosome Mapping
• Chromosomes, Human, Pair 6
• Female
• Genetic Linkage
• Genetic Markers
• Humans
• Macular Degeneration (genetics)
• Male
• North Carolina
• Pedigree
• Phenotype