Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen

Am J Hum Genet. 1992 Aug;51(2):235-44.


Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides from type I procollagen. Initially identified in cattle more than 20 years ago, the disorder was subsequently characterized in sheep, cats, and dogs. Affected animals have fragile skin, lax joints, and often die prematurely because of sepsis following avulsion of portions of skin. We recently identified two children with soft, lax, and fragile skin, which, when examined by transmission electron microscopy, contained the twisted, ribbon-like collagen fibrils characteristic of dermatosparaxis. Skin extracts from one child contained collagen precursors with amino-terminal extensions. Cultured fibroblasts from both children failed to cleave the amino-terminal propeptides from the pro alpha 1(I) and pro alpha 2(I) chains in type I procollagen molecules. Extracts of normal cells cleaved to collagen, the type I procollagen synthesized by cells from both children, demonstrating that the enzyme, not the substrate, was defective. These findings distinguish dermatosparaxis from Ehlers-Danlos syndrome type VII, which results from substrate mutations that prevent proteolytic processing of type I procollagen molecules.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acids / metabolism
  • Cells, Cultured
  • Collagen / biosynthesis
  • Collagen / genetics
  • Collagen / isolation & purification
  • Ehlers-Danlos Syndrome / classification
  • Ehlers-Danlos Syndrome / genetics
  • Ehlers-Danlos Syndrome / metabolism
  • Ehlers-Danlos Syndrome / pathology*
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Fibroblasts / metabolism
  • Genetic Complementation Test
  • Humans
  • Hydrolysis
  • Infant
  • Microscopy, Electron
  • Procollagen / genetics
  • Procollagen / metabolism*
  • RNA Processing, Post-Transcriptional
  • Skin / metabolism
  • Skin / ultrastructure


  • Amino Acids
  • Procollagen
  • Collagen