A case of hidrotic ectodermal dysplasia with developing eccrine syringofibroadenoma with heterozygous mutation of GJB6 gene

J Dermatol. 2022 Dec;49(12):e451-e452. doi: 10.1111/1346-8138.16565. Epub 2022 Sep 2.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Connexin 30 / genetics
  • Ectodermal Dysplasia* / diagnosis
  • Ectodermal Dysplasia* / genetics
  • Humans
  • Mutation
  • Poroma*
  • Sweat Gland Neoplasms*

Substances

  • Connexin 30
  • GJB6 protein, human