Clinical and histopathologic signs of iris nevus (Cogan-Reese) syndrome

Objective & Hypothesis:Iris nevus (Cogan Reese) syndrome, Chandler syndrome and Progressive iris Atrophy are studied as Iridocorneal Endothelial syndromes.

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Key Findings & Data:Iris Nevus (Cogan Reese) syndrome is characterized by unilateral glaucoma and iris nodules.

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Conclusion & Impact:Clinical and histopathologic signs are presented in a 37 year old case diagnosed as Iris Nevus (Cogan Reese) syndrome.

🔬Design:Research Article

📍Scope:Comprehensive Sample

⚙️Variables:İris neoplazmları · Glokom · İris hastalıkları

Abstract

Iris nevus (Cogan Reese) syndrome, Chandler syndrome and Progressive iris Atrophy are studied as Iridocorneal Endothelial syndromes. Iris Nevus (Cogan Reese) syndrome is characterized by unilateral glaucoma and iris nodules. Clinical and histopathologic signs are presented in a 37 year old case diagnosed as Iris Nevus (Cogan Reese) syndrome.

Özet

İris nevüs (Cogan-Reese} sendromu, Chandler sendromu ve Progresif iris atrofisi iridokorneal Endotelyal Sendromlar başlığı altında incelenir. İris Nevüs (Cogan Reese)Sendromu tek taraflı glokom ve iris nodülleri ile karakterize bir klinik tablodur. İris Nevüs (Cogan Reese) Sendromu tanısı konulan 37 yaşındaki erkek hastada saptanan klinik ve histopatolojik bulgular tartışılmıştır.

Keywords

İris neoplazmları Glokom İris hastalıkları Sendrom açık-açılı Kornea ödemi Iris Neoplasms Glaucoma Iris Diseases Syndrome Open-Angle Corneal Edema

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Cite This Article

ÖZDEMİR, Y., ÖNDER, F., KURAL, G. (1999). Clinical and histopathologic signs of iris nevus (Cogan-Reese) syndrome. MN Oftalmoloji, Cilt: 6 - Sayı: 3, 292–294. https://ajindex.com/articles/296537