Choroidal neovascularization in Bardet-Biedl syndrome

Leon D. Charkoudian, David E. Barañano, Jorge Fortun, Jiong Yan, Sunil K. Srivastava

Research output: Contribution to journalArticle

Abstract

Purpose: To describe a case of choroidal neovascularization in a young patient with genetically-proven Bardet-Biedl syndrome. Methods: Case description with fundus and anatomical photography and optical coherence tomography. Patients: Single patient case description. Results: Fundus photography and optical coherence tomography reveal the presence of previously-active choroidal neovascularization. Anatomical, historical, and genetic evidence confirm Bardet-Biedl syndrome in this individual. Discussion: Choroidal neovascularization accompanying this syndrome has not been reported. Herein we describe the first published description of choroidal neovascularization in an individual with genetically-proven Bardet-Biedl syndrome.

Original languageEnglish (US)
Pages (from-to)52-54
Number of pages3
JournalOphthalmic Genetics
Volume34
Issue number1-2
DOIs
StatePublished - Mar 1 2013
Externally publishedYes

Keywords

  • Bardet-Biedl
  • Choroid
  • Neovascularization
  • Polydactyly
  • Syndrome

ASJC Scopus subject areas

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

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  • Cite this

    Charkoudian, L. D., Barañano, D. E., Fortun, J., Yan, J., & Srivastava, S. K. (2013). Choroidal neovascularization in Bardet-Biedl syndrome. Ophthalmic Genetics, 34(1-2), 52-54. https://doi.org/10.3109/13816810.2011.603404