Familial neurofibromatosis type 1 has diverse manifestations in skin and is associated with steatocystoma multiplex

Clin Exp Dermatol. 2021 Aug;46(6):1166-1169. doi: 10.1111/ced.14618. Epub 2021 Apr 19.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Exome Sequencing
  • Genes, Neurofibromatosis 1
  • Humans
  • Male
  • Mutation
  • Neurofibromatosis 1 / complications*
  • Neurofibromatosis 1 / genetics*
  • Neurofibromatosis 1 / pathology
  • Pedigree
  • Steatocystoma Multiplex / complications*
  • Steatocystoma Multiplex / genetics*
  • Steatocystoma Multiplex / pathology
  • Young Adult