'Double trouble': diagnostic challenges in genetic skin disorders

Br J Dermatol. 2015 Jan;172(1):276-8. doi: 10.1111/bjd.13159. Epub 2014 Dec 17.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anodontia / diagnosis
  • Anodontia / genetics*
  • Breast / abnormalities*
  • Child
  • Dermatitis, Exfoliative / diagnosis
  • Dermatitis, Exfoliative / genetics*
  • Ectodermal Dysplasia / diagnosis
  • Ectodermal Dysplasia / genetics*
  • Female
  • Heterozygote
  • Humans
  • Lacrimal Duct Obstruction / diagnosis
  • Lacrimal Duct Obstruction / genetics*
  • Limb Deformities, Congenital / diagnosis
  • Limb Deformities, Congenital / genetics*
  • Male
  • Mutation / genetics*
  • Nails, Malformed / diagnosis
  • Nails, Malformed / genetics*
  • Pigmentation Disorders / diagnosis
  • Pigmentation Disorders / genetics*
  • Skin Diseases / congenital
  • Transcription Factors / genetics*
  • Transglutaminases / genetics*
  • Tumor Suppressor Proteins / genetics*

Substances

  • TP63 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins
  • transglutaminase 5
  • Transglutaminases

Supplementary concepts

  • Peeling skin syndrome, acral type
  • Propping Zerres syndrome