Probable autosomal dominant optic atrophy with hearing loss

Marilyn Baird Mets*, Ernest Mhoon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


The seventh family manifesting an entity described as automosal dominant optic atrophy with hearing loss is reported here. This disorder shows great inter-and intrafamilial variation in the onset time and the degree of loss of both vision and hearing. Unlike autosomal dominant optic atrophy without hearing loss, it appears to be associated with a red-green (deutan) defect in color vision.

Original languageEnglish (US)
Pages (from-to)85-89
Number of pages5
JournalOphthalmic Paediatrics and Genetics
Issue number1-2
StatePublished - Jan 1 1985


  • Deutan color defect
  • Optic atrophy with hearing loss

ASJC Scopus subject areas

  • Genetics(clinical)
  • Ophthalmology
  • Pediatrics, Perinatology, and Child Health


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