Familial primary localized cutaneous amyloidosis in a Japanese family

J Dermatol Sci. 2016 Aug;83(2):162-4. doi: 10.1016/j.jdermsci.2016.05.007. Epub 2016 May 11.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Amyloidosis, Familial / genetics*
  • Amyloidosis, Familial / metabolism
  • Exome
  • Female
  • Humans
  • Immunohistochemistry
  • Keratin-14 / metabolism
  • Keratin-5 / metabolism
  • Keratin-6 / metabolism
  • Mutation, Missense
  • Oncostatin M Receptor beta Subunit / genetics*
  • Sequence Analysis, DNA
  • Serum Amyloid P-Component / analysis
  • Skin Diseases, Genetic / genetics*
  • Skin Diseases, Genetic / metabolism

Substances

  • KRT14 protein, human
  • KRT5 protein, human
  • Keratin-14
  • Keratin-5
  • Keratin-6
  • OSMR protein, human
  • Oncostatin M Receptor beta Subunit
  • Serum Amyloid P-Component

Supplementary concepts

  • Amyloidosis, Primary Cutaneous