Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation

Br J Dermatol. 2016 Dec;175(6):1369-1371. doi: 10.1111/bjd.14694. Epub 2016 Sep 27.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Humans
  • Hyperpigmentation / genetics*
  • Hyperpigmentation / pathology
  • Hypopigmentation / genetics*
  • Hypopigmentation / pathology
  • Male
  • Mutation, Missense / genetics*
  • Stem Cell Factor / genetics*

Substances

  • Stem Cell Factor