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Hearing disability in patients with Fuchs’ endothelial corneal dystrophy: unrecognized co-pathology?

By Marilette Stehouwer, Ward R Bijlsma and Allegonda Van der Lelij
Topics: Original Research
Publisher: Dove Medical Press
OAI identifier: oai:pubmedcentral.nih.gov:3180502
Provided by: PubMed Central

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Citations

  1. (2005). Borate transport and cell growth and proliferation. Not only in plants. Cell Cycle.
  2. Borate transporter SLC4 A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
  3. Classification of corneal endothelial disorders based on neural crest origin.
  4. Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13.
  5. (1999). Diabetes and hearing impairment in the United States: audiometric evidence from the National Health and Nutrition Examination Survey,
  6. (1988). Diagnostic performance of the hearing handicap inventory for the elderly (screening version) against differing definitions of hearing loss. Ear Hear.
  7. (1990). Discriminating and responsiveness abilities of two hearing handicap scales. Ear Hear.
  8. (1910). Dystrophia epithelialis corneae. Albrecht Von Graefes Arch Klin Exp Ophthalmol.
  9. (1999). Fuchs’ endothelial dystrophy: a fresh look at an aging disease. Ophthalmic Physiol Opt.
  10. (1983). Identification of elderly people with hearing problems.
  11. (2005). Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy. Invest Ophthalmol Vis Sci.
  12. (1994). Methods for screening for hearing loss in older adults.
  13. (2006). Mutations in sodiumborate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nat Genet.
  14. Prevalence and risk factors for cornea guttata in the Reykjavik Eye Study.
  15. Prevalence of and risk factors for cornea guttata in a population-based study in a southwestern island of Japan: the Kumejima study.
  16. Regeneration with proliferation of the endothelium of cultured human donor corneas with extended postmortem time.
  17. (2008). SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Hum Mol Genet.
  18. SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria.
  19. Validation of screening tools for identifying hearing-impaired elderly in primary care.
  20. Validation of self-reported hearing loss. The Blue Mountains Hearing Study.
  21. (1986). Validity of a screening protocol for identifying elderly people with hearing problems.