Evaluation of visual function and needs in adult patients with Bardet-Biedl syndrome

  • Alastair K. Denniston*
  • , Philip L. Beales
  • , Paul J. Tomlins
  • , Peter Good
  • , Maria Langford
  • , Lukas Foggensteiner
  • , Denise Williams
  • , Marie D. Tsaloumas
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose: To assess the visual needs of the adult population with Bardet-Biedl syndrome (BBS) and to ensure that this is addressed by a national Bardet-Biedl Service. Methods: A cross-sectional analysis of all adults under a national BBS Clinic (Birmingham, United Kingdom) was performed using the BBS Ophthalmic Assessment Tool, a novel tool designed to capture the key elements of visual function, impact on lifestyle, and clinical findings relevant to BBS. Results: Sixty-two adult patients were confirmed to have BBS. Bardet-Biedl syndrome mutations were identified in 51, most commonly BBS1 (n = 35), BBS2 (n = 6), and BBS10 (n = 5). In 11 patients (18%), BBS had not been diagnosed until adulthood. Median visual acuity was hand motion (range, 0.0 logMAR-no perception of light). More advanced retinopathy was associated with increasing age, worsening visual acuity, and the presence of nystagmus. Forty patients (65%) had undertaken mainstream education with 29 (47%) achieving higher education; 7 patients (11%) had moderate or severe learning difficulties. Most (90%) were registered sight-impaired or severely sight-impaired patients. Conclusion: The BBS Ophthalmic Assessment Tool provides a wide-ranging assessment of ophthalmic status and vision-related needs of the BBS population. This evaluation demonstrates the spectrum of visual disability in this population and its correlation with worsening retinopathy over time.

Original languageEnglish
Pages (from-to)2282-2289
Number of pages8
JournalRetina
Volume34
Issue number11
DOIs
Publication statusPublished - 1 Nov 2014

Bibliographical note

Publisher Copyright:
© Ophthalmic Communications Society, Inc.

Keywords

  • Bardet-Biedl syndrome
  • Ciliopathy
  • Ophthalmic genetics
  • Retinal dystrophy

ASJC Scopus subject areas

  • Ophthalmology

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