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Journals / Retina-Vitreus / 2005 / Cilt: 13 - Sayı: 2

Examining of two cases with congenital retinoschisis

Konjenital retinoskizisli iki olgunun irdelenmesi

Orhan AYDEMİR
Turgut YILMAZ
Mehmet BALBABA
Pages
143–146
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this report, we examined the clinical features and the characteristical findings in two cases of congenital retinoschisis

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Purpose: Congenital hereditary retinoschisis, or juvenile X linked retinoschisis, is a bilateral vitreoretinal dystrophy that devolops early in life.
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Key Findings & Data:It is seen between the ages of 5-10, predominantly in males.
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Conclusion & Impact:In this report, we examined the clinical features and the characteristical findings in two cases of congenital retinoschisis
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Görme keskinliği · Ergen · Çocuk

Abstract

Purpose: Congenital hereditary retinoschisis, or juvenile X linked retinoschisis, is a bilateral vitreoretinal dystrophy that devolops early in life. It is a relatively rare disease. It is seen between the ages of 5-10, predominantly in males. In this report, we examined the clinical features and the characteristical findings in two cases of congenital retinoschisis

Özet

Amaç: Konjenital herediter retinoskizis veya bir başka isimle jüvenil X'e bağlı retinoskizis, hayatın erken döneminde ortaya çıkan, bilateral tutulum gösteren bir vitreoretinal distrofidir. Oldukça nadir görülen bir hastalıktır. Hastalık sıklıkla 5-10 yaş arasında ve erkeklerde gözlenmektedir. Bu çalışmada konjenital retinoskizis tanısı alan iki olgunun klinik bulguları ve karakteristik özellikleri incelendi.

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Cite This Article

AYDEMİR, O., YILMAZ, T., BALBABA, M. (2005). Examining of two cases with congenital retinoschisis. Retina-Vitreus, Cilt: 13 - Sayı: 2, 143–146. https://ajindex.com/articles/305324

References (10)

  1. Ödland M.: Congenital retinoschisis. Acta Ophthalmol 1981; 59:649-658
  2. Berinstein DM, Hiraoka M, Trese MT, et al.: Coats' disease and congenital retinoschisis in a single eye: a case report and DNA analysis. Ophthalmologica 2001; 215:132-135
  3. Condon GP, Brownstein S, Wang NS, et al.: Congenital hereditary (juvenile X-linked) retinoschisis. Histopathologic and ultrastructural findings in three eyes. Arch Ophthalmol 1986; 104:576-583
  4. Sebates FN.: Juvenile retinoschisis. Am J Ophthalmol 1966; 62:683-688
  5. Apaydın KC, Acar A.: Travmatik total oftalmopleji ve juvenil retinoskizis: Bir olgu sunumu. T Oft Gaz 1988;18:364-373
  6. Miyake Y, Shiroyama N, Ota I, et al.: Focal macular electroretinogram in X-linked congenital retinoschisis. Invest Ophthalmol Vis Sei 1993; 34:512-515
  7. Forsius H, Krause U, Helve J, et al.: Visual acuity in 183 cases of X-chromosomal retinoschisis. Can J Ophthalmol 1993; 8:385-393
  8. Yanoff M, Kertesz Rahn E, Zimmerman LE.: Histopathology of juvenile retinoschisis. Arch Ophthalmol 1968; 79:49-53
  9. Kellner U, Brummer S, Foerster MH, et al.: X-linked congenital retinoschisis. Greafe's Arch Clin Exp Ophthalmol 1990; 228:432-437
  10. Gopal L, Shanmugam MP, Battu RR, et al.: Congenital retinoschisis: successful collapse with photocoagulation. Indian J Ophthalmol 2001; 49:265-266.