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TGFBI Mutational Analysis in a New Zealand Population of Inherited Corneal Dystrophy Patients
  1. Andrea L Vincent*,
  2. Betina de Karolyi,
  3. Dipika V Patel,
  4. Catherine E Wheeldon,
  5. Charles NJ McGhee
  1. 1 Department of Ophthalmology, University of Auckland, New Zealand
  1. Correspondence to: Andrea L Vincent, Ophthalmology, University of Auckland, Faculty of Medical and health Sciences, Private Bag 92019, Victoria St West, Auckland, 1142, 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. We aim to characterize 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 (CGD) had the R555W mutation, and H626P was identified in an intermediate dystrophy of Bowman layer (CBD) 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 characterized. No mutations were identified in some individuals/pedigrees suggesting greater genetic heterogeneity than is currently known in this group of disorders.

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