Report of a family with dominantly inherited upper lid entropion

Br J Ophthalmol. 2000 Nov;84(11):1303-5. doi: 10.1136/bjo.84.11.1303.

Abstract

Aim: To report the occurrence of late onset, bilateral, idiopathic upper lid entropion, occurring in three members of the same family, with a known family history.

Methods: Five family members were examined, and a history taken, at Moorfields Eye Hospital. Three patients were treated surgically, and one also had a tarsoconjunctival biopsy.

Results: In all cases, no aetiology was found. The family history suggests an autosomal dominant inheritance pattern. All patients were treated with anterior lamellar repositioning, and had optimal results.

Conclusion: The family reported seems to be affected by a familial form of primary acquired upper lid entropion, that shows an autosomal dominant inheritance pattern.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Biopsy
  • Entropion / genetics*
  • Entropion / surgery
  • Female
  • Humans
  • Male
  • Pedigree
  • Treatment Outcome