What is megalocornea?
Megalocornea is a rare condition in which the diameter of the cornea (the clear layer at the front of the eye) is larger than normal. The condition is present at birth and is more common in males than females. It may be isolated or accompanied by other symptoms.
The condition is usually bilateral and symmetrical. This means both eyes are affected equally. Megalocornea is also non-progressive, meaning it should not worsen or change over time.
Though the diameter in megalocornea is large, other features like corneal thickness, steepness and clarity are usually normal. Intraocular pressure is also within normal range.
There is no cure or treatment for the anatomical defect of megalocornea. However, there are methods to treat and manage complications associated with the condition. These complications can include refractive error, lens dislocation, retinal detachment and glaucoma, among others.
In most cases, megalocornea is caused by an X-linked recessive mutation in gene CHRDL 1. An “X-linked recessive mutation” means a problem lies within a gene located on the X chromosome. Because males only have one X chromosome, they are much more likely to have megalocornea than females.
A mutation in CHRDL 1 causes the anterior segment of the eye to be enlarged (anterior megalophthalmos). Experts have developed a few theories on why this enlargement occurs.
The CHRDL 1 gene codes for a protein called ventropin. Ventropin helps regulate the production of bone morphogenetic proteins (BMPs). These proteins are involved in corneal growth.
A mutation in CHRDL 1 causes an absence of ventropin and leads to unregulated corneal growth. This causes a delay in optic cup fusion — an important process that occurs during embryo development. The delay in fusion gives more time for corneal growth, which results in a larger-than-average cornea and anterior segment.
Megalocornea can also be caused by an autosomal mutation. This means the mutated gene is located on a numbered chromosome, not a sex chromosome (X or Y).
There are other less common theories behind what could cause megalocornea. These include:
Congenital glaucoma was in the beginning stages of development, then stopped.
The enlarged anterior chamber is caused by abnormal collagen synthesis.
Conditions associated with megalocornea
When there are other findings besides megalocornea, it’s likely because an underlying condition is present. In this case, megalocornea is part of a syndrome rather than its own isolated condition.
Some conditions associated with megalocornea include:
Alport syndrome – A genetic disease that causes progressive kidney disease, along with inner ear and eye abnormalities.
Marfan syndrome – A genetic disorder that affects the connective tissue throughout the body.
Ehlers-Danlos syndrome – A genetic condition that affects the formation and function of collagen.
Down syndrome – A genetic disorder that causes varying physical and intellectual disabilities.
Frank-Ter Haar syndrome – An inherited disease characterized by many physical abnormalities and developmental delays.
Boucher-Neuhäuser syndrome – A genetic disorder that affects movement, vision and sexual development. Also known as megalocornea intellectual disability syndrome.
Signs and symptoms of megalocornea
The main sign of megalocornea is having corneas with larger-than-normal diameters.
The average diameter of a cornea is 11.04 to 12.50 millimeters (mm) for males and 10.70 to 12.58 mm for females. An eye with megalocornea has a corneal diameter of 13 mm or greater.
Internal structures of the eye may look different to compensate for the larger cornea. These changes include:
The anterior chamber of the eye is deeper.
The vitreous chamber of the eye is shallower.
Iridocorneal angles are wider and more open than normal.
The trabecular meshwork shows excessive pigmentation.
Other signs and symptoms may include light sensitivity and cornea globosa (misshapen cornea). If complications of megalocornea arise, related symptoms may be experienced.
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Complications of megalocornea
In some cases, megalocornea may not have any effect on vision. However, it’s possible for complications of varying degrees to occur. These complications may include:
Refractive errors are imperfections within the eye that affect how it focuses light, which results in blurry vision. Two refractive errors that may develop as a complication of megalocornea are myopia and astigmatism.
Myopia, or nearsightedness, is a condition in which distant objects appear blurry while close-up objects are clear. It occurs when light entering the eye falls in front of the retina rather than directly on it.
Astigmatism is caused by irregularities in the shape of the cornea or lens. The irregularities cause incoming light to scatter instead of focus on the retina. This produces a fuzzy or distorted image, and can affect the ability to see clearly at near and far distances.
Refractive errors are very common and easily corrected with prescription eyeglasses or contact lenses.
Lens dislocation occurs when the lens of the eye becomes displaced from its normal location. If the lens is subluxed, it means it’s partially displaced, but still in the lens space. With a luxated (dislocated) lens, the lens is completely detached and floating freely elsewhere in the eye.
When the lens becomes displaced, a condition called iridodonesis may occur. It’s characterized by the iris vibrating during eye movements. This results from the lens detaching from its suspensory ligaments.
Complications during cataract surgery are also more likely with megalocornea. The plastic lens that is placed inside the eye after the cataract is removed (called an intraocular lens implant) can become dislocated. This happens because the suspensory ligaments and the membrane that holds the intraocular lens in place can rupture. Because the dimensions of an eye with megalocornea are different, special types of intraocular lenses may need to be used during cataract surgery.
This is a medical emergency and should be treated promptly to avoid vision damage or loss.
Arcus juvenilis describes a condition called arcus senilis when it occurs in babies and young children. Arcus senilis is a condition in which a white, light gray or bluish ring appears around the edge of the cornea. The ring is made up of fatty lipids (cholesterol).
The condition is usually asymptomatic and does not affect vision; however, a doctor will need to check for any underlying conditions.
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It’s possible to have no symptoms associated with corneal dystrophy, but most types worsen over time and can cause vision loss.
Glaucoma is a disease characterized by high intraocular pressure that ultimately damages the optic nerve. It occurs when eye fluid (called aqueous humor) is produced more quickly than it can be drained, which raises pressure within the eye.
The condition can be sight-threatening, but it’s treatable with different prescription medications.
A cataract is a clouding of the eye’s lens that can interfere with vision. It’s caused by the breakdown and clumping of proteins in the lens, which happens naturally with age.
If left untreated, cataracts can cause vision loss. Fortunately, cataract surgery is very common and widely available for patients who need it.
Treatment, management and prognosis
There is no treatment for the anatomical defect of megalocornea. Rather, treatment and management refer to the issues that can stem from the condition.
If megalocornea is an isolated case, the most common treatment needed is for refractive errors. This can typically be done with corrective lenses. Managing the condition requires regular eye exams that allow your eye doctor to track potential problems like glaucoma or cataracts.
In the case of cataract surgery, patients with megalocornea may require a special intraocular lens, and special precautions may be needed to allow for a successful outcome.
Megalocornea that is a symptom of an underlying condition will likely require more attention and treatment than an isolated case. Discuss any concerns with your doctor, who can advise you on the best treatment for your situation.
Prognosis for megalocornea depends on whether it’s associated with another disease. If another condition is responsible for your megalocornea, it’s best to research the details for that particular disease.
However, if isolated, the prognosis for megalocornea is positive. As long as the proper correction and treatment are taken, people with the condition can live life with clear vision.
Megalocornea. EyeWiki. American Academy of Ophthalmology. January 2022.
Megalocornea. American Academy of Ophthalmology. Accessed August 2022.
Megalocornea. StatPearls. July 2022.
What are the different ways a genetic condition can be inherited? MedlinePlus. April 2021.
Autosomal dominant & autosomal recessive. Cleveland Clinic. May 2022.
Alport syndrome. National Organization for Rare Disorders. 2020.
Marfan syndrome. American Association for Pediatric Ophthalmology & Strabismus. April 2020.
Ehlers Danlos syndrome. StatPearls. June 2022.
About Down syndrome. National Down Syndrome Society. Accessed August 2022.
Frank Ter Haar syndrome: About the disease. Genetic and Rare Diseases Information Center. November 2021.
Boucher-Neuhäuser syndrome. MedlinePlus. October 2016.
White-to-white corneal diameter: Normal values in healthy humans obtained with the orbscan ii topography system. The Journal of Cornea and External Disease. April 2005.
Isolated congenital megalocornea. Orphanet. Accessed August 2022.
Astigmatism. National Eye Institute. June 2019.
Ectopia lentis. EyeWiki. American Academy of Ophthalmology. March 2022.
What is iridodonesis? News Medical. March 2019.
Retinal detachment. National Eye Institute. April 2022.
What is arcus senilis? American Academy of Ophthalmology. April 2019.
Corneal dystrophies. National Eye Institute. June 2019.
What is glaucoma? Symptoms, causes, diagnosis, treatment. American Academy of Ophthalmology. September 2021.
Cataracts. National Eye Institute. April 2022.
Page published on Tuesday, September 13, 2022
Medically reviewed on Monday, August 29, 2022