Three autosomal dominant corneal dystrophies map to chromosome 5q.

E M Stone, W D Mathers, G O Rosenwasser, E J Holland, R Folberg, J H Krachmer, B E Nichols, P D Gorevic, C M Taylor, L M Streb
Author Information
  1. E M Stone: Department of Ophthalmology, University of Iowa College of Medicine, Iowa City 52242.

Abstract

The two most common autosomal dominant dystrophies of the corneal stroma are lattice corneal dystrophy type I and granular dystrophy. A third autosomal dominant stromal dystrophy (Avellino) has also been recognized. Chromosome linkage analysis of four families with Avellino dystrophy mapped the disease-causing gene to chromosome 5q. Subsequent linkage analysis of two families with typical lattice dystrophy and two with typical granular dystrophy also revealed significant linkage with the same markers. Thus, each of three clinically and histopathologically distinct phenotypes is independently linked to 5q. The maximum combined lod score using all 114 affected patients was 28.6 with marker D5S393. None of the 14 known human amyloid-associated genes map to chromosome 5.

Grants

  1. EY08426/NEI NIH HHS
  2. HG00457/NHGRI NIH HHS
  3. P50HG00835/NHGRI NIH HHS

MeSH Term

Alleles
Amyloid
Chromosome Mapping
Chromosomes, Human, Pair 5
Corneal Dystrophies, Hereditary
Female
Genes, Dominant
Genetic Linkage
Genetic Markers
Humans
Italy
Lod Score
Male
Pedigree
United States

Chemicals

Amyloid
Genetic Markers

Word Cloud

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