Dominant congenital deafness and progressive optic nerve atrophy. Occurrence in four generations of a family

Arch Ophthalmol. 1974 Feb;91(2):99-103. doi: 10.1001/archopht.1974.03900060105003.
No abstract available

MeSH terms

  • Audiometry
  • Child
  • Color Perception Tests
  • Color Vision Defects / etiology
  • Deafness / congenital*
  • Deafness / genetics
  • Female
  • Fundus Oculi
  • Genes, Dominant
  • Humans
  • Male
  • Middle Aged
  • Optic Atrophy / genetics*
  • Pedigree
  • Scotoma / etiology
  • Syndrome