Megalocornea: Difference between revisions

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{{Infobox medical condition
| name            = Megalocornea
| synonyms        = Anterior megalophthalmos
| field          = [[Ophthalmology]]
| symptoms        = Enlarged [[cornea]], [[myopia]], [[astigmatism]]
| complications  = [[Glaucoma]], [[cataract]]
| onset          = Congenital
| duration        = Lifelong
| causes          = Genetic mutations, often [[X-linked recessive]]
| risks          = Family history of the condition
| diagnosis      = [[Ophthalmic examination]], [[corneal diameter]] measurement
| differential    = [[Buphthalmos]], [[keratoglobus]]
| treatment      = Corrective lenses, monitoring for complications
| prognosis      = Generally good with management of complications
| frequency      = Rare
}}
'''Megalocornea''' is a rare, non-progressive [[eye disorder]] characterized by an abnormally large [[cornea]]. The cornea is the clear, dome-shaped surface that covers the front of the [[eye]]. In individuals with megalocornea, the diameter of the cornea is typically more than 13 millimeters, compared to the average diameter of 11.5 to 12 millimeters.
'''Megalocornea''' is a rare, non-progressive [[eye disorder]] characterized by an abnormally large [[cornea]]. The cornea is the clear, dome-shaped surface that covers the front of the [[eye]]. In individuals with megalocornea, the diameter of the cornea is typically more than 13 millimeters, compared to the average diameter of 11.5 to 12 millimeters.
==Causes==
==Causes==
Megalocornea is usually an inherited condition, passed down in families through an [[X-linked recessive]] pattern of inheritance. This means that the condition is caused by a mutation in a gene on the X chromosome. The most common gene associated with megalocornea is the CHRDL1 gene.
Megalocornea is usually an inherited condition, passed down in families through an [[X-linked recessive]] pattern of inheritance. This means that the condition is caused by a mutation in a gene on the X chromosome. The most common gene associated with megalocornea is the CHRDL1 gene.
==Symptoms==
==Symptoms==
The primary symptom of megalocornea is an abnormally large cornea. Other symptoms can include [[nystagmus]] (involuntary eye movement), [[astigmatism]] (blurred vision due to an irregularly shaped cornea), and [[myopia]] (nearsightedness). However, vision is typically not significantly affected in individuals with megalocornea.
The primary symptom of megalocornea is an abnormally large cornea. Other symptoms can include [[nystagmus]] (involuntary eye movement), [[astigmatism]] (blurred vision due to an irregularly shaped cornea), and [[myopia]] (nearsightedness). However, vision is typically not significantly affected in individuals with megalocornea.
==Diagnosis==
==Diagnosis==
Megalocornea is typically diagnosed through a comprehensive eye examination. This can include a [[slit lamp examination]], which allows the doctor to examine the structures at the front of the eye under magnification. Other diagnostic tests can include [[corneal topography]], which maps the surface of the cornea, and [[optical coherence tomography]] (OCT), which provides cross-sectional images of the eye.
Megalocornea is typically diagnosed through a comprehensive eye examination. This can include a [[slit lamp examination]], which allows the doctor to examine the structures at the front of the eye under magnification. Other diagnostic tests can include [[corneal topography]], which maps the surface of the cornea, and [[optical coherence tomography]] (OCT), which provides cross-sectional images of the eye.
==Treatment==
==Treatment==
There is no cure for megalocornea, and treatment is typically focused on managing any associated symptoms. This can include prescription glasses or contact lenses to correct astigmatism or myopia. In some cases, surgery may be required to correct associated conditions such as [[glaucoma]] or [[cataracts]].
There is no cure for megalocornea, and treatment is typically focused on managing any associated symptoms. This can include prescription glasses or contact lenses to correct astigmatism or myopia. In some cases, surgery may be required to correct associated conditions such as [[glaucoma]] or [[cataracts]].
==See also==
==See also==
* [[Cornea]]
* [[Cornea]]
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* [[X-linked recessive inheritance]]
* [[X-linked recessive inheritance]]
* [[CHRDL1]]
* [[CHRDL1]]
[[Category:Eye disorders]]
[[Category:Eye disorders]]
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]

Latest revision as of 03:33, 4 April 2025


Megalocornea
Synonyms Anterior megalophthalmos
Pronounce N/A
Specialty N/A
Symptoms Enlarged cornea, myopia, astigmatism
Complications Glaucoma, cataract
Onset Congenital
Duration Lifelong
Types N/A
Causes Genetic mutations, often X-linked recessive
Risks Family history of the condition
Diagnosis Ophthalmic examination, corneal diameter measurement
Differential diagnosis Buphthalmos, keratoglobus
Prevention N/A
Treatment Corrective lenses, monitoring for complications
Medication N/A
Prognosis Generally good with management of complications
Frequency Rare
Deaths N/A


Megalocornea is a rare, non-progressive eye disorder characterized by an abnormally large cornea. The cornea is the clear, dome-shaped surface that covers the front of the eye. In individuals with megalocornea, the diameter of the cornea is typically more than 13 millimeters, compared to the average diameter of 11.5 to 12 millimeters.

Causes[edit]

Megalocornea is usually an inherited condition, passed down in families through an X-linked recessive pattern of inheritance. This means that the condition is caused by a mutation in a gene on the X chromosome. The most common gene associated with megalocornea is the CHRDL1 gene.

Symptoms[edit]

The primary symptom of megalocornea is an abnormally large cornea. Other symptoms can include nystagmus (involuntary eye movement), astigmatism (blurred vision due to an irregularly shaped cornea), and myopia (nearsightedness). However, vision is typically not significantly affected in individuals with megalocornea.

Diagnosis[edit]

Megalocornea is typically diagnosed through a comprehensive eye examination. This can include a slit lamp examination, which allows the doctor to examine the structures at the front of the eye under magnification. Other diagnostic tests can include corneal topography, which maps the surface of the cornea, and optical coherence tomography (OCT), which provides cross-sectional images of the eye.

Treatment[edit]

There is no cure for megalocornea, and treatment is typically focused on managing any associated symptoms. This can include prescription glasses or contact lenses to correct astigmatism or myopia. In some cases, surgery may be required to correct associated conditions such as glaucoma or cataracts.

See also[edit]

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