Familial progressive hyper- and hypopigmentation caused by a novel mutation in site II of the KITLG gene

J Dermatol. 2021 Sep;48(9):e462-e463. doi: 10.1111/1346-8138.16016. Epub 2021 Jun 11.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Albinism, Oculocutaneous*
  • Humans
  • Hyperpigmentation* / diagnosis
  • Hyperpigmentation* / genetics
  • Hypopigmentation* / diagnosis
  • Hypopigmentation* / genetics
  • Male
  • Mutation
  • Stem Cell Factor / genetics*

Substances

  • KITLG protein, human
  • Stem Cell Factor