Corneal involvement in a case of autosomal dominant Stargardt-like macular dystrophy (STGD3) with ELOVL4 mutation

Ophthalmic Genet. 2022 Feb;43(1):134-136. doi: 10.1080/13816810.2021.1983848. Epub 2021 Oct 1.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Eye Proteins / genetics
  • Humans
  • Macular Degeneration* / congenital
  • Macular Degeneration* / genetics
  • Membrane Proteins / genetics
  • Mutation
  • Retinal Dystrophies*

Substances

  • ELOVL4 protein, human
  • Eye Proteins
  • Membrane Proteins

Supplementary concepts

  • Stargardt disease 3