Haber's syndrome may be a clinical entity different from Dowling-Degos disease

Br J Dermatol. 2009 Jan;160(1):215-7. doi: 10.1111/j.1365-2133.2008.08938.x. Epub 2008 Nov 28.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Chromosome Disorders / genetics
  • Chromosome Disorders / pathology*
  • Class I Phosphatidylinositol 3-Kinases
  • Diagnosis, Differential
  • Female
  • Humans
  • Hyperpigmentation / genetics
  • Hyperpigmentation / pathology
  • Keratin-5 / genetics*
  • Keratosis, Seborrheic / genetics
  • Keratosis, Seborrheic / pathology*
  • Pedigree
  • Phosphatidylinositol 3-Kinases / genetics
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics
  • Skin Diseases / genetics
  • Skin Diseases / pathology*
  • Syndrome
  • Treatment Outcome

Substances

  • KRT5 protein, human
  • Keratin-5
  • Phosphatidylinositol 3-Kinases
  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CA protein, human
  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3