Polycoria

Polycoria is extremely rare, and other conditions are frequently mistaken for it.[2][3] Polycoria is often congenital, however not diagnosed until adulthood.[4] The general cause of polycoria is unknown, but there are some other eye conditions that are in association with polycoria. These include (although not often) polar cataracts, glaucoma, abnormally long eyelashes, abnormal eye development, and poor vision.[5]

There have been cases diagnosed from age 3 to adulthood. The prevalence of true polycoria is minimal.[3] The two kinds of polycoria are true polycoria and false pseudopolycoria.

There are no known or proposed trends in the occurrences of polycoria based on geographical location, age, gender, or season.

In cases of true polycoria, there is an extra pupil that tends to be reactive to light and medication.[6] To be considered true polycoria the extra pupil and the principal pupil must dilate and contract simultaneously with triggers such as light and administered drugs.[7] The extraneous pupil is c. 2.5mm away from the principal pupil. In cases of true polycoria there is an intact sphincter muscle, which contracts and dilates the pupils.[6] In an eye without polycoria, the sphincter muscle is a part of the iris that functions to constrict and dilate the pupil.[8] A patient with true polycoria experiences handicapped vision as well as stimulation of the retina in response to bright lights.[6]

It is said that the term "true polycoria" is overused, and used correctly when addressing congenital deformations of the iris.[7] Often "true polycoria" is used when it in fact is a case of pseudopolycoria.

Although less rare than true polycoria, pseudopolycoria is still very uncommon. In cases of pseudopolycoria there is a "passive constriction" that differentiates the extra pupil from the true pupil during constriction and dilation. The extra pupil in pseudopolycoria is different than the extra pupil in true polycoria because it shows defects that are independent of the sphincter muscles.[5] Pseudopolycoria is often associated with Seckel syndrome, posterior polymorphous dystrophy, and juvenile glaucoma.[6]

Pseudopolycoria consists of splitting of the iris that are not contingent with the sphincter muscles at the root of the iris.[7]

When a patient is diagnosed with polycoria, the signs and symptoms shown are associated with ocular and adexal growth abnormalities.[9] The iris and the pupil become less effective. Signs can be present as a child; however, the patient may be diagnosed later in their life. This condition results in abnormal eye development affecting both eyes or just one.[10]

Upon gross examination the patient will typically have excessively long eyelashes.[9] The iris becomes hypoplastic, making abnormally shaped pupils with prominent crypts.[9] The crypts are little squiggly lines that radiate out around the pupil; with this condition, thick round or oval openings can be seen.[9]

On diagnosis, signs lead to symptoms where there is more than one set of iris muscles, which controls the amount of light being brought into the eye.[9] When the iris becomes deformed, it will disarrange the control of light coming in leading to blurred vision and finding it hard to visually focus. Polar cataracts will also be present in this condition where a round, opaque malformation of distorted lens fibers is located in the central posterior part of the lens showing disformality.[11] Blindess may also be caused due to damage of the optic nerve from glaucoma.[10]

Polycoria has been linked to hereditary genetics,[9] and also associated with polar cataracts, glaucoma, and retinal detachment.[6] Not all cases are treated for this iris abnormality, but when cases are treated the only treatment is surgical procedure and life-long ocular monitoring that is highly recommended.[12] Considerations for surgery are surgical correction, intraocular surgery, and/or reapproximation, as if it was being treated for glaucoma or retinal detachment.[12] Children under the age of 3, who do not seek surgical surgery, have responded well with miotic drops that contained mydriatic/cycloplegic, allowing the separate eye sphincters to dilate and constrict together. This allows improved balance of uncorrected visual acuity.[13] A 1-mm limbal incisions would be made, a spatula is inserted through the side to elevate the two pupils (avoiding contact with the lens), and the iris tissue would be cut using viscoelastic material. Finally, the limbal incisions were closed with stromal hydration, and intracameral cefuroxime is applied.[6]

There is no current known preventative measures for polycoria, however genetic testing may be able to reveal genetic patterns of the disorder.[5] Conditions such as reduced corneal thickness, are observed in people with cases of polycoria, as well as keratoconus (keratoconus is a corneal disease has the possibility of leading to blindness and/or astigmatism).[19][5] However, there are some proposals that it is caused by a dissociation of the pupil margins, a partial coloboma which is a hole in the eye, or abnormal eye tissue composition.[6]

As of now, there is not any known direct mechanisms involved in the development of true polycoria or pseudopolycoria. There are some proposed ideas, one being that after the sphincter muscle is fully formed and developed in the eye there is a severing of the pupillary margins leading to the distinction of the extra pupil and the principal pupil.[7] Polycoria can also be caused any hole in one's iris to develop a sphincter muscle development.[7] Another proposed theory about the cause of polycoria is intra-uterine trauma, or postpartum iris trauma.[7]

If the development of the iris is hindered, the ectoderm of the eye (which forms the lens and corneal epithelium) may split, which could lead to pseudopolycoria.[7]

The gene that is the cause of this disorder is the PRDM5 gene.[12] The PRDM5 gene has also been linked to Brittle Cornea syndrome, which is a tissue disorder of the eye, as well as Axenfeld syndome.[12] PRDM5 plays crucial roles in the molecular composition of the eye, as well as the tissue thickness.[12] Axenfeld syndrome occurs in the patient in a case of the mutation of the FOXC1 gene, which is a heterozygous mutation.[12]

Since true polycoria and pseudopolycoria are so rare, there is not much history on the disorders. According to an article published in 2002, there have only been 2 cases of true polycoria since 1966.[3]

• Eye injury
• Iridodialysis
• Monocular diplopia
• Coloboma