Case of hypohidrotic ectodermal dysplasia caused by a large deletion mutation in the EDA gene

J Dermatol. 2013 Apr;40(4):281-3. doi: 10.1111/1346-8138.12077. Epub 2013 Jan 7.
No abstract available

Publication types

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

MeSH terms

  • Asian People
  • Ectodermal Dysplasia 1, Anhidrotic / genetics*
  • Ectodysplasins / genetics*
  • Humans
  • Infant
  • Male
  • Pedigree
  • Polymerase Chain Reaction
  • Sequence Deletion / genetics*

Substances

  • EDA protein, human
  • Ectodysplasins