Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene

J Dermatol. 2011 Dec;38(12):1205-8. doi: 10.1111/j.1346-8138.2011.01265.x. Epub 2011 Sep 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Alopecia / complications*
  • Alopecia / genetics*
  • Basal Cell Nevus Syndrome / complications*
  • Basal Cell Nevus Syndrome / genetics*
  • Basal Cell Nevus Syndrome / pathology
  • Female
  • Humans
  • Middle Aged
  • Patched Receptors
  • Patched-1 Receptor
  • Receptors, Cell Surface / genetics*
  • Sequence Deletion

Substances

  • PTCH1 protein, human
  • Patched Receptors
  • Patched-1 Receptor
  • Receptors, Cell Surface