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TGFBI mutational analysis in a New Zealand population of inherited corneal dystrophy patients
  1. Andrea L Vincent1,2,
  2. Betina de Karolyi1,
  3. Dipika V Patel1,2,
  4. Catherine E Wheeldon1,2,
  5. Charles N J McGhee1,2
  1. 1Department of Ophthalmology, Faculty of Medical and Health Sciences, National Eye Centre, University of Auckland, Auckland, New Zealand
  2. 2Eye Clinic, Greenlane Clinical Centre, Auckland District Health Board, Auckland, New Zealand
  1. Correspondence to Dr Andrea Vincent, Department of Ophthalmology, University of Auckland, Private Bag 92019, Auckland, New Zealand; a.vincent{at}auckland.ac.nz

Abstract

Aim The corneal dystrophies represent a group of clinically and genetically heterogeneous, inherited diseases, often resulting in bilateral opacification of the cornea, and may require penetrating keratoplasty. Mutations in the transforming growth factor beta-induced (TGFBI) gene segregate with a wide range of phenotypically heterogeneous corneal dystrophies. Many of the other dystrophies remain without molecular characterisation. This study aimed to characterise the molecular basis for corneal disease in a New Zealand population.

Methods Nineteen unrelated individuals affected with a corneal dystrophy (granular, fleck, lattice, posterior polymorphous) and their family members were recruited, a pedigree obtained and their dystrophy extensively phenotyped. After informed consent, samples were taken for DNA extraction. PCR and sequencing of all coding exons of TGFBI was undertaken.

Results All five patients with granular dystrophy had the R555W mutation, and H626P was identified in an intermediate dystrophy of Bowman layer pedigree. No other mutations were detected including in the stromal dystrophy cases.

Conclusion Mutational analysis of TGFBI in a small population has identified sequence changes consistent with previously identified genotype–phenotype correlations. A new genotype–phenotype association was also characterised. No mutations were identified in some individuals/pedigrees suggesting greater genetic heterogeneity than is currently known in this group of disorders.

  • Cornea
  • corneal dystrophies
  • diagnostic tests/investigations
  • genetics
  • hereditary
  • mutation
  • TGFBI

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Footnotes

  • Funding This work was funded by the Save Sight Society of New Zealand, University of Auckland Research Committee.

  • Competing interests None.

  • Patient consent Obtained.

  • Ethics approval This study was conducted with the approval of the Northern X Regional Ethics Committee, Ministry of Health (NTX06/121/61, and AKX/02/00/002) and Auckland District Health Board Research Review Committee (A+3657).

  • Provenance and peer review Not commissioned; externally peer reviewed.

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