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In a healthy eye, the cornea has a smooth, round shape that allows light to focus precisely on the retina. In keratoconus, the cornea becomes thinner and weaker over time, causing it to bulge forward and become irregular.
This irregular shape disrupts the eye’s focusing ability and can lead to increasing levels of astigmatism and short-sightedness.
Keratoconus typically affects both eyes, although one eye may progress more rapidly than the other. The condition often begins around puberty and may continue to progress into early adulthood.
While the exact cause is not always clear, keratoconus has been associated with:
With appropriate monitoring and treatment, many patients maintain functional vision for many years.
Symptoms often develop gradually and may include:
As the condition progresses, glasses may become less effective at correcting vision.
If keratoconus is suspected, a comprehensive corneal assessment is recommended. Early diagnosis is important, as treatments are available to slow or halt progression and help maintain visual quality. Management focuses on both stabilising the cornea and improving visual clarity.
Diagnosis typically involves detailed imaging of the cornea, including:
These tests allow early detection of corneal changes and help guide appropriate treatment planning.
Keratoconus treatment depends on severity and may include vision correction or procedures to stabilise the cornea.
Recovery varies depending on the treatment performed.
For crosslinking procedures:
For kerarings or corneal graft procedures:
With early intervention and structured care, the progression of keratoconus can often be successfully controlled.