A missense mutation in type VII collagen in two affected siblings with recessive dystrophic epidermolysis bullosa

Nat Genet. 1993 May;4(1):62-6. doi: 10.1038/ng0593-62.

Abstract

Recessive dystrophic epidermolysis bullosa is a severe mutilating genodermatosis. Previous ultrastructural demonstrations of altered anchoring fibrils, and recent genetic linkage analyses have suggested that type VII collagen, the major component of anchoring fibrils, is a candidate gene. We have identified a homozygous methionine-to-lysine mutation in two affected siblings, while their unaffected mother and half-brother are heterozygous carriers. The mutation resides in a highly conserved region of the C-terminus of type VII collagen, strongly suggesting that it is the cause of the disease in this family.

Publication types

  • Case Reports
  • Comparative Study

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Child
  • Collagen / genetics*
  • Consanguinity
  • Cricetinae
  • DNA Mutational Analysis
  • Epidermolysis Bullosa Dystrophica / genetics*
  • Female
  • Genes, Recessive
  • Homozygote
  • Humans
  • Male
  • Mice
  • Molecular Sequence Data
  • Mutation*
  • Pedigree
  • Phylogeny
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Species Specificity

Substances

  • Collagen