Segregation of all four major fibrillar collagen genes in the Marfan syndrome

Am J Hum Genet. 1987 Dec;41(6):1071-82.

Abstract

Linkage markers at or close to the genes encoding the three major fibrillar collagens were used to analyze the segregation of these loci in six pedigrees with dominantly inherited Marfan syndrome. Four pedigrees were discordant at one of the Type I collagen loci (COL1A2), and, of these, two were discordant at the other Type I locus (COL1A1). The Marfan syndrome also segregated independently of the structural loci for Type II and Type III collagen in these two families. This is evidence against the Marfan syndrome being, in general, due to mutations in the major fibrillar collagen genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Collagen / genetics*
  • Female
  • Genes*
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Male
  • Marfan Syndrome / genetics*
  • Pedigree
  • Recombination, Genetic

Substances

  • Genetic Markers
  • Collagen