Genetics of Keratoconus: Where Do We Stand?
Генетика кератоконуса: на каком этапе мы находимся?
2014-01-01
SCID: 54.1/5yzjp9gm
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candidate genescorneal thinninggenetic risk factorsgenome-wide associationkeratoconus
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Abstract (AI)
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.
Key Findings
1
Genome-wide and candidate-gene studies have identified several genomic loci and genes associated with keratoconus susceptibility.
2
Its pathophysiology has a complex multifactorial basis involving environmental, behavioral, and multiple genetic components.
3
Keratoconus is a progressive corneal disorder involving thinning, anterior protrusion, steepening, refractive distortion, and reduced vision.
4
The identified genetic factors support a complex molecular etiology rather than a single-gene cause of keratoconus.
5
The review summarizes current knowledge of genetic risk factors associated with keratoconus.
Research Object
Keratoconus
Research Subject
Genetic risk factors and molecular etiology of keratoconus
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Publication Date
2014-01-01
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