Visual Impairment Secondary to Unilateral Isolated Epicapsular Star
We aimed to report a rarely observed case of unilateral epicapsular star and the visual impairment developed secondary to it. A 8-year-old girl presented with a complaint of blurred vision in the right eye; best-corrected visual acuity was 0.7 in the right eye and 1.0 in the left eye. Near visual...
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| Language: | English |
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Galenos Publishing House
2014-12-01
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| Series: | Türk Oftalmoloji Dergisi |
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| Online Access: | http://www.oftalmoloji.org/article_7556/Visual-Impairment-Secondary-To-Unilateral-Isolated-Epicapsular-Star |
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| author | Mehmet Serhat Mangan Mehmet Erdoğan Eray Atalay |
| author_facet | Mehmet Serhat Mangan Mehmet Erdoğan Eray Atalay |
| author_sort | Mehmet Serhat Mangan |
| collection | DOAJ |
| description | We aimed to report a rarely observed case of unilateral epicapsular star and the visual impairment developed secondary to it. A 8-year-old
girl presented with a complaint of blurred vision in the right eye; best-corrected visual acuity was 0.7 in the right eye and 1.0 in the left
eye. Near visual acuity was J1 in the right eye and J1+ in the left eye. The patient had no systemic disease and no clinical findings such
as ocular inflammation, trauma, or history of use of topical and systemic drug. On biomicroscopic examination, no pigment deposition
was observed in the cornea of both eyes and anterior chamber was normal. The anterior capsule of the lens in the right eye demonstrated
dense pigment depositions centrally which were obscuring the pupillary axis. Iris translumination defect was not seen. Gonioscopy was
performed and no pigment deposition was seen in the iridocorneal angle. Fundus examination revealed no pathology in the vitreous,
posterior pole, and peripheral retina. In the absence of signs of intraocular inflammation and other causes of primary or secondary
pigment dispersion, it is likely that the pigmented cells were implanted on the lens surface in utero from the developing iris pigment
epithelium. In such cases, visual impairment should be detected in early period, and the strict follow-up is of utmost importance. (Turk
J Ophthalmol 2014; 44: 493-5) |
| format | Article |
| id | doaj-art-3c6fd54ded674989a0d40f73f4fa43ce |
| institution | Kabale University |
| issn | 1300-0659 2147-2661 |
| language | English |
| publishDate | 2014-12-01 |
| publisher | Galenos Publishing House |
| record_format | Article |
| series | Türk Oftalmoloji Dergisi |
| spelling | doaj-art-3c6fd54ded674989a0d40f73f4fa43ce2025-08-20T03:55:37ZengGalenos Publishing HouseTürk Oftalmoloji Dergisi1300-06592147-26612014-12-0144649349510.4274/tjo.02360Visual Impairment Secondary to Unilateral Isolated Epicapsular StarMehmet Serhat Mangan0 Mehmet Erdoğan1Eray Atalay2Muş Devlet Hastanesi, Göz Hastalıkları Kliniği, Muş, Türkiyeİstanbul Üniversitesi Cerrahpaşa Tıp Fakültesi, Göz Hastalıkları Anabilim Dalı, İstanbul, TürkiyeKars Devlet Hastanesi, Göz Hastalıkları Kliniği, Kars, TürkiyeWe aimed to report a rarely observed case of unilateral epicapsular star and the visual impairment developed secondary to it. A 8-year-old girl presented with a complaint of blurred vision in the right eye; best-corrected visual acuity was 0.7 in the right eye and 1.0 in the left eye. Near visual acuity was J1 in the right eye and J1+ in the left eye. The patient had no systemic disease and no clinical findings such as ocular inflammation, trauma, or history of use of topical and systemic drug. On biomicroscopic examination, no pigment deposition was observed in the cornea of both eyes and anterior chamber was normal. The anterior capsule of the lens in the right eye demonstrated dense pigment depositions centrally which were obscuring the pupillary axis. Iris translumination defect was not seen. Gonioscopy was performed and no pigment deposition was seen in the iridocorneal angle. Fundus examination revealed no pathology in the vitreous, posterior pole, and peripheral retina. In the absence of signs of intraocular inflammation and other causes of primary or secondary pigment dispersion, it is likely that the pigmented cells were implanted on the lens surface in utero from the developing iris pigment epithelium. In such cases, visual impairment should be detected in early period, and the strict follow-up is of utmost importance. (Turk J Ophthalmol 2014; 44: 493-5)http://www.oftalmoloji.org/article_7556/Visual-Impairment-Secondary-To-Unilateral-Isolated-Epicapsular-StarEpicapsular starcongenital lenticular pigmentationvisual impairment |
| spellingShingle | Mehmet Serhat Mangan Mehmet Erdoğan Eray Atalay Visual Impairment Secondary to Unilateral Isolated Epicapsular Star Türk Oftalmoloji Dergisi Epicapsular star congenital lenticular pigmentation visual impairment |
| title | Visual Impairment Secondary to Unilateral Isolated Epicapsular Star |
| title_full | Visual Impairment Secondary to Unilateral Isolated Epicapsular Star |
| title_fullStr | Visual Impairment Secondary to Unilateral Isolated Epicapsular Star |
| title_full_unstemmed | Visual Impairment Secondary to Unilateral Isolated Epicapsular Star |
| title_short | Visual Impairment Secondary to Unilateral Isolated Epicapsular Star |
| title_sort | visual impairment secondary to unilateral isolated epicapsular star |
| topic | Epicapsular star congenital lenticular pigmentation visual impairment |
| url | http://www.oftalmoloji.org/article_7556/Visual-Impairment-Secondary-To-Unilateral-Isolated-Epicapsular-Star |
| work_keys_str_mv | AT mehmetserhatmangan visualimpairmentsecondarytounilateralisolatedepicapsularstar AT mehmeterdogan visualimpairmentsecondarytounilateralisolatedepicapsularstar AT erayatalay visualimpairmentsecondarytounilateralisolatedepicapsularstar |