Genetics of Keratoconus: Where Do We Stand?

Author:

Abu-Amero Khaled K.123,Al-Muammar Abdulrahman M.1,Kondkar Altaf A.12

Affiliation:

1. Ophthalmic Genetics Laboratory, Department of Ophthalmology, College of Medicine, King Saud University, P.O. Box 245, Riyadh 11411, Saudi Arabia

2. Glaucoma Research Chair, Department of Ophthalmology, College of Medicine, King Saud University, P.O. Box 245, Riyadh 11411, Saudi Arabia

3. Department of Ophthalmology, College of Medicine, University of Florida, Jacksonville, FL 32209, USA

Abstract

Keratoconus is a progressive thinning and anterior protrusion of the cornea that results in steepening and distortion of the cornea, altered refractive powers, and reduced vision. Keratoconus has a complex multifactorial etiology, with environmental, behavioral, and multiple genetic components contributing to the disease pathophysiology. Using genome-wide and candidate gene approaches several genomic loci and genes have been identified that highlight the complex molecular etiology of this disease. The review focuses on current knowledge of these genetic risk factors associated with keratoconus.

Funder

King Saud University

Publisher

Hindawi Limited

Subject

Ophthalmology

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