Ultrastructural Investigations in an Autosomal Recessively Inherited Case of Dyschromatosis Universalis Hereditaria

Acta Derm Venereol. 2015 Jul;95(6):738-40. doi: 10.2340/00015555-2030.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Epidermis / enzymology
  • Epidermis / ultrastructure
  • Humans
  • Intramolecular Oxidoreductases / genetics
  • Keratinocytes / ultrastructure*
  • Male
  • Melanocytes / ultrastructure*
  • Melanosomes / ultrastructure*
  • Membrane Glycoproteins / genetics
  • Microscopy, Electron, Transmission
  • Monophenol Monooxygenase / genetics
  • Oxidoreductases / genetics
  • Pigmentation Disorders / congenital*
  • Pigmentation Disorders / genetics
  • Pigmentation Disorders / pathology
  • RNA, Messenger / analysis
  • Skin Diseases, Genetic / genetics
  • Skin Diseases, Genetic / pathology*
  • Young Adult

Substances

  • Membrane Glycoproteins
  • RNA, Messenger
  • Oxidoreductases
  • TYRP1 protein, human
  • Monophenol Monooxygenase
  • Intramolecular Oxidoreductases
  • dopachrome isomerase

Supplementary concepts

  • Dyschromatosis universalis hereditaria