A novel form of "central pouchlike" cataract, with sutural opacities, maps to chromosome 15q21-22

Am J Hum Genet. 2001 Feb;68(2):509-14. doi: 10.1086/318189. Epub 2000 Dec 21.


Congenital cataract is a clinically and genetically highly heterogeneous eye disorder, with autosomal dominant inheritance being most common. We investigated a large seven-generation family with 74 individuals affected by autosomal dominant congenital cataract (ADCC). The phenotype in this family can be described as "central pouchlike" cataract with sutural opacities, and it differs from the other mapped cataracts. We performed linkage analysis with microsatellite markers in this family and excluded the known candidate genes. A genomewide search revealed linkage to markers on chromosome 15, with a maximum two-point LOD score of 5.98 at straight theta=0 with marker D15S117. Multipoint analysis also gave a maximum LOD score of 5.98 at D15S117. Multipoint and haplotype analysis narrowed the cataract locus to a 10-cM region between markers D15S209 and D15S1036, closely linked to marker D15S117 in q21-q22 region of chromosome 15. This is the first report of a gene for a clinically new type of ADCC at 15q21-22 locus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cataract / congenital
  • Cataract / genetics*
  • Cataract / pathology
  • Chromosome Mapping
  • Chromosomes, Human, Pair 15 / genetics*
  • Family Health
  • Female
  • Genetic Linkage
  • Haplotypes
  • Humans
  • Lod Score
  • Male
  • Microsatellite Repeats
  • Molecular Sequence Data
  • Pedigree

Associated data

  • OMIM/121015
  • OMIM/123580
  • OMIM/123610
  • OMIM/123620
  • OMIM/123680
  • OMIM/123690
  • OMIM/131220
  • OMIM/134797
  • OMIM/134920
  • OMIM/148180
  • OMIM/164950
  • OMIM/176943
  • OMIM/600825
  • OMIM/600897
  • OMIM/602669
  • OMIM/603212