![]() |
NIOEYES.COM The Definitive
Ophthalmic Server
|
|
Eye
Problems,Causes, Prevention, Tests, Treatments, Consulting your Doctor |
| Keratoconus | ||
| Table of Contents | ||
| Alternative
Names Conical Cornea |
||
| Defination Keratoconus, also known as Conical Cornea, is a non-inflammatory condition of the cornea in which there is progressive central thinning of the cornea changing it from dome-shaped to cone-shaped. Keratoconus comes from the Greek word meaning ConicalCornea (Cone shaped- Cornea). The cornea is the clear windshield of the eye and is responsible for refracting most of the light coming into the eye. Therefore, abnormalities of the cornea can severely affect the way we see the world, including simple tasks such as: driving, watching TV, or reading a book. Keratoconus is not a blinding disorder, per se, but does result in a greatly increasing near-sightedness (things far away are out of focus) and irregular astigmatism (things look tilted) that can significantly distort your vision. It is almost always bilateral (affecting both eyes). It is a slowly progressive disorder, taking years to develop, and may halt at any stage from mild to severe. |
||
| Causes,
Incidence and Risk Factors Although there is some research, the underlying reason for its development remains obscure. Some cases of KC have a hereditary component and studies indicate that about 8% of patients have affected relatives. However, most cases appear to be sporadic. It occurs in all ethnic groups and has a slight female preponderance. The cause of Keratoconus remains unknown. Keratoconus is not generally considered an inherited disorder, but the chance of a blood relative having Keratoconus is thought to be as high as one in 10. Vigorous eye rubbing, although not the cause of Keratoconus, can contribute to the disease process. Therefore, patients with Keratoconus are advised to avoid rubbing their eyes. Keratoconus usually has its onset in puberty with progression over a 10 to 20 year period. This rate of progression is variable as well as the severity, ranging from mild astigmatism to severe corneal thinning, protrusion, and scarring. Keratoconus has been associated with other medical disorders including atopic disease, Down's syndrome, Ehlers-Danlos syndrome, Marfan's syndrome, craniofacial dysostosis and osteogenesis imperfecta. Even excessive eye rubbing and contact lens wear has been implicated in this disease |
||
| Prevention |
||
| Symptoms Blurring and distortion of vision are the earliest symptoms of Keratoconus. Symptoms usually appear in the late teens or early twenties. The disease will often progress slowly for 10 to 20 years, and then usually stop. In the early stages, vision may be only slightly affected, causing glare, light sensitivity and irritation. Each eye may be affected differently. As the disease progresses and the cornea steepness and scars, vision may become distorted. Then, you may experience one or more the following symptoms: Halos, ghosting, cloudy vision, double vision, and pain Rarely, a sudden decrease in vision can occur if the cornea swells (corneal hydrops). The cornea swells when the elastic part of the cornea develops a tiny crack, created by the strain of the cornea's protruded cone-like shape. The swelling may persist for weeks or months as the crack heals and is gradually replaced by scar tissue. Patients with KC initially notice visual blurring and distortion. This may be accompanied by photophobia (light sensitivity) and glare. Patients may note the need for frequent changes in their glasses. In the advanced stages, there may be a precipitous drop in vision due to clouding of the cornea, referred to an acute corneal hydrops. This condition usually resolves over weeks to months, but is often followed by central corneal scarring |
||
| Signs
& Tests |
||
| Treatment Depends on the severity of the condition. Initially, eyeglasses are often successful in correcting the myopia (near sightedness) and astigmatism; however, as the disease advances vision is not adequately corrected and requires rigid contact lenses to aid in flattening the corneal surface and providing optimal visual correction. Contact lens fitting can be difficult in patients with KC requiring frequent visits and lens changes but recent advances in the contact lens industry as provided more fitting options. Lastly, when good vision can no longer be attained with contact lenses or intolerance to the contact lens develops, corneal transplantation is recommended. This is only necessary in about 10% of patients with KC and carries a success rate of greater than 90%, one of the highest for corneal transplantation. Although this procedure replaces the thinned central portion of the cornea, eyeglasses and contact lenses are often required for maximal visual acuity. |
||
| Expectations
(Prognosis) |
||
| Complications |
||
| Calling
your doctor/health care provider |
||
|
Disclaimer |
| The information contained above is intended for general reference purposes only. It is not a substitute for professional medical advice or a medical exam. Always seek the advice of your physician or other qualified health professional before starting any new treatment. Medical information changes rapidly and while NIO and its content providers make efforts to update the content on the site, some information may be out of date. No health information on NIO, including information about herbal therapies and other dietary supplements, is regulated or evaluated by the Health Ministry of the Government of India and therefore the information should not be used to diagnose, treat, cure or prevent any disease without the supervision of a medical doctor. |