Pellucid Marginal Degeneration

Pellucid Marginal Degeneration commonly referred to as PMD or even just Pellucid, is an extremely rare degenerative corneal eye condition. The Term Pellucid Marginal Degeneration was first coined by an ophthalmologist named Schalaeppi in 1957. Pellucid Marginal Degeneration by definition is a bilateral thinning in the periphery of the cornea, that is not inflammatory, however unilateral cases have been reported.

A little more information about Pellucid Marginal Degeneration is that it is actually unknown how many instances of PMD there actually occur every year. PMD is extremely rare; however the main contributing factor to the unknown instance count is greatly due to its confusion with keratoconus, which is another more common eye disorder.


Keratoconus is sometimes confused with PMD because it is also a degenerative eye disorder, however in keratoconus patients there are changes within the cornea that cause it to thin and change to a more cone shape instead of the normal gradual cure that normal eyes have.

Most literature states that Pellucid Marginal Degeneration is not painful, and that no symptoms actually accompany the condition other than the obvious visual deterioration. The lack of pain however has not been the case for me. You can read more about my struggle with PMD here.

Early signs of PMD are virtual non-existent. When the eye is exampled by an optometrist or an ophthalmologist, the patients corneal thickness appears normal in the center, also showing an intact central epithelium. However the inferior cornea exhibits a peripheral band of thinning. When a patient has PMD there is a high astigmatism, along with horizontal bow ties, and inferior peripheral thinning between the 7 and 4 o’clock meridian. Here is a picture of that.

Thinning of the inferior cornea.

Thinning of the inferior cornea.

 

Pellucid Marginal Degeneration has had no identifiable factors linking reace, sex, or age. Almost all reported cases however have been early in life between the ages of 20 – 40. No known cause for the disease has been found. The most common element that leads to the discovery of PMD in a patient is the rapid visual decline due to the irregular corneal shape. This always will lead to a very bad astigmatism, and therefore creates extremely distorted vision. Overtime the deterioration and distortion will become more sever.

Due to the changes in the shape of the eye Pellucid rules patients out for many different types of eye surgeries such as refractive surgery, LASIK surgery, and PRK surgery. Another interesting point to note about PMD is that visual aids such as glasses do not work for pellucid due to the changed shape of the eye, vision will still be distorted.

{ 5 comments… read them below or add one }

samson hwata January 23, 2012 at 3:06 pm

All the literature i have read says this disease is not hereditary. I want to disagree because my mothers two sisters have this codition. One was operated on and she has since gone blind. The other had an intact inserted in one eye and she is waiting for a cornea translant in the other. I have to go thru the same process for my eyes but due to financial constrains this cannot be done. Please confirm that this condition is not hereditary. I am in ZIMBABWE my phone no is 2630774502118.

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Aaron February 2, 2012 at 8:08 am

become more sever.

should be

become more severe.

Just diagnosed with pmd. Probably had it for years, misdiagnosed with keratoconus. New prescription is helping. I can finally read with my bad eye.

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Tommy February 9, 2012 at 11:13 pm

Just diagnosed with PMD myself today after over 10 years of being told I had karatoconus. What’s also strange is that I too only have symptoms in 1 eye instead of both, which my doctor said was very rare. So what prescription did you finally get to help you? Are you in a special soft lens or a hard lens?

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Lan Serpas February 8, 2012 at 4:24 am

Can I take part of your content to my personal web site? Thanks.

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James February 10, 2012 at 10:08 pm

of course feel free to use any of this information a reference link would be appreciated but is not necessary.

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