Iris and fundus pigmentary changes in tuberous sclerosis

N. J. Lucchese, M. F. Goldberg

Research output: Contribution to journalArticlepeer-review

Abstract

Tuberous sclerosis is a rare, dominantly inherited phakomatosis that is characterized by epilepsy, mental deficiency, and adenoma sebaceum. Retinal hamartomas are typical ocular findings. The reported incidence of such lesions varies from about 4 to 53%. Although iris depigmentation is known to occur in tuberous sclerosis, this is, to our knowledge, the first report of extensive fundus pigmentary changes in a patient with this disease.

Original languageEnglish (US)
Pages (from-to)45-46
Number of pages2
JournalJournal of pediatric ophthalmology and strabismus
Volume18
Issue number6
StatePublished - 1981
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Ophthalmology

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