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Journal articles on the topic 'Cogan-Reese Syndrome'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Holló, Gábor, Péter Kóthy, and Anastasios G. P. Konstas. "Association of Cogan-Reese Syndrome, Exfoliation Syndrome, and Secondary Open-Angle Glaucoma." European Journal of Ophthalmology 22, no. 1 (2011): 117–20. http://dx.doi.org/10.5301/ejo.5000047.

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Purpose To present a case with co-existence of Cogan-Reese syndrome and exfoliation syndrome. Case report A 72-year-old Caucasian woman presented for consultation due to uncontrolled intraocular pressure (IOP) of the right eye. Clinical examination revealed the presence of Cogan-Reese syndrome and exfoliation syndrome OD. This eye exhibited elevated IOP, open anterior chamber angle, advanced glaucomatous optic nerve head damage, and severe glaucomatous visual field loss. The left eye was completely normal without IOP elevation or visual field damage. To our knowledge this is the first case rep

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2

Tester, Robert A. "Cogan-Reese Syndrome." Archives of Ophthalmology 116, no. 8 (1998): 1126. http://dx.doi.org/10.1001/archopht.116.8.1126.

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3

Khushi, Kansal* Hiba Khan. "Formulation And Evaluation of Herbal Ointment Containing Neem and Turmeric." International Journal of Pharmaceutical Sciences 3, no. 4 (2025): 2228–35. https://doi.org/10.5281/zenodo.15237016.

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Cogan-Reese Syndrome is a rare and progressive ocular disorder classified under iridocorneal endothelial (ICE) syndromes, primarily affecting middle-aged females. It is characterized by abnormal corneal endothelial proliferation leading to distinct iris changes and secondary glaucoma. This case report details the clinical presentation, diagnostic approach, and management of a 42-year-old female diagnosed with CRS and secondary angle-closure glaucoma. The patient presented with progressive diminution of vision in her right eye over two months, with a history of prior glaucoma diagnosis and medi

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4

Behera, Geeta, TapasC Nag, SudarshanK Khokhar, and Suneel Sangaraju. "Electron microscopy in Cogan–Reese syndrome." Indian Journal of Ophthalmology 70, no. 7 (2022): 2666. http://dx.doi.org/10.4103/ijo.ijo_2777_21.

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5

Bouvarel, Hugo, Pascale Hamard, Emilie Agard, Jérémy Billant, Hussam El Chehab, and Corinne Dot. "Macular edema in Cogan-Reese syndrome." American Journal of Ophthalmology Case Reports 25 (March 2022): 101318. http://dx.doi.org/10.1016/j.ajoc.2022.101318.

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6

Kumar, Dr Mrs Kavita, and Dr Rashmi Ingale. "Iridocorneal endothelial syndrome: Cogan -Reese syndrome. A case report." International Journal of Medical Research and Review 1, no. 5 (2013): 261–63. http://dx.doi.org/10.17511/ijmrr.2013.i05.08.

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7

Selvan, Harathy, Anand S. Brar, and Dewang Angmo. "Cogan-Reese syndrome with Iris cyst: A novel presentation." Contact Lens and Anterior Eye 42, no. 4 (2019): 467–69. http://dx.doi.org/10.1016/j.clae.2019.04.014.

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8

Harvey, Ben J., Hans E. Grossniklaus, Matthew P. Traynor, Steven R. Sarkisian, and Donald U. Stone. "Metastatic Lung Adenocarcinoma to the Iris Mimicking Cogan-Reese Syndrome." Journal of Glaucoma 21, no. 8 (2012): 567–69. http://dx.doi.org/10.1097/ijg.0b013e3182208a2e.

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9

Rao, Aparna. "Cogan Reese Syndrome, a Unilateral Puzzling Cause of Secondary Glaucoma." Ophthalmology Glaucoma 3, no. 4 (2020): 287. http://dx.doi.org/10.1016/j.ogla.2020.02.004.

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10

Özdemir, Yildiz, Feyza Önder, C. Banu Coşar, Alp Usubütün, and Gülcan Kural. "Clinical and histopathologic findings of iris nevus (Cogan-Reese) syndrome." Acta Ophthalmologica Scandinavica 77, no. 2 (1999): 234–37. http://dx.doi.org/10.1034/j.1600-0420.1999.770226.x.

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11

Huna, Ruth, Adiel Barak, and Shlomo Melamed. "Bilateral Iridocorneal Endothelial Syndrome Presented as Cogan-Reese and Chandler??s Syndrome." Journal of Glaucoma 5, no. 1 (1996): 60???62. http://dx.doi.org/10.1097/00061198-199602000-00010.

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12

Rath, Archana, Sumita Mohapatra, Rakesh A. Betdur, and Harshvardhan V. K. "Medical and surgical management has a role in control of intraocular pressure in early detected iridocorneal endothelial syndrome: case series." International Journal of Advances in Medicine 4, no. 2 (2017): 589. http://dx.doi.org/10.18203/2349-3933.ijam20171065.

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Iridocorneal endothelial syndrome is a rare ocular disorder characterized by abnormal endothelization of angle structure and iris producing characteristic manifestation including secondary angle closure glaucoma. The purpose is to present four cases of iridocorneal endothelial syndrome with glaucoma and discuss clinical presentation and management strategies. Out of four cases, two cases of Cogan-Reese syndrome who present early have well controlled IOP with trabeculectomy with mitomycin-C. One case who presented late with progressive iris atrophy and secondary angle closure glaucoma went to a

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13

Holló, Gábor, and Farzaneh Naghizadeh. "Optical Coherence Tomography Characteristics of the Iris in Cogan-Reese Syndrome." European Journal of Ophthalmology 24, no. 5 (2014): 797–99. http://dx.doi.org/10.5301/ejo.5000465.

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14

Gutiérrez-Ortiz, C., J. Pareja, G. Bolívar, M. T. Cedazo, J. I. Busteros, and M. A. Teus. "Iris Melanocytoma Mimicking the Cogan-Reese Syndrome with Monocular Pigment Dissemination." European Journal of Ophthalmology 16, no. 6 (2006): 873–75. http://dx.doi.org/10.1177/112067210601600617.

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15

Senthilkumar, Vijayalakshmi A., Sujitha Ramesh, and George V. Puthuran. "Management of refractory glaucoma in Cogan–Reese variant of ICE syndrome with secondary tube implantation." Indian Journal of Ophthalmology - Case Reports 4, no. 1 (2024): 59–61. http://dx.doi.org/10.4103/ijo.ijo_1058_23.

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Glaucoma secondary to iridocorneal endothelial syndrome is refractory to medical treatment, and its management is always challenging. We report the clinical course and management of refractory glaucoma in a 47-year-old male diagnosed with Cogan–Reese syndrome with an 11-year follow-up result. He initially underwent trabeculectomy, which eventually failed after 7 years; hence, an Aurolab aqueous drainage implant (AADI) was placed superotemporally. On subsequent follow-up, as the AADI tube got retracted, secondary AADI implantation was placed in the superonasal quadrant. Later, his vision droppe

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16

Chakrabarty, Lipi. "A unique case of keratoconus with Cogan-Reese syndrome and secondary glaucoma." Indian Journal of Ophthalmology 65, no. 1 (2017): 64. http://dx.doi.org/10.4103/ijo.ijo_986_15.

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17

Loya-Garcia, Denise. "Cogan-Reese syndrome: image analysis with specular microscopy, optical coherence tomography, and ultrasound biomicroscopy." Digital Journal of Ophthalmology 25, no. 2 (2019): 26. http://dx.doi.org/10.5693/djo.02.2019.05.001.

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18

Sacchetti, Marta, Flavio Mantelli, Marco Marenco, Ilaria Macchi, Oriella Ambrosio, and Paolo Rama. "Diagnosis and Management of Iridocorneal Endothelial Syndrome." BioMed Research International 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/763093.

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The iridocorneal endothelial (ICE) syndrome is a rare ocular disorder that includes a group of conditions characterized by structural and proliferative abnormalities of the corneal endothelium, the anterior chamber angle, and the iris. Common clinical features include corneal edema, secondary glaucoma, iris atrophy, and pupillary anomalies, ranging from distortion to polycoria. The main subtypes of this syndrome are the progressive iris atrophy, the Cogan-Reese syndrome, and the Chandler syndrome. ICE syndrome is usually diagnosed in women in the adult age. Clinical history and complete eye ex

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19

Krasińska, Aleksandra, Joanna Mamczur, Manuela Pajdowska, and Agata Brązert. "Difficulties in Treatment of Iridocorneal Endothelial Syndrome - Case Report." Medical Journal of Cell Biology 10, no. 2 (2022): 56–60. http://dx.doi.org/10.2478/acb-2022-0009.

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Abstract The iridocorneal endothelial syndrome manifests in three clinical types: Chandler syndrome, progressive iris atrophy, and Cogan-Reese syndrome. It is caused by the presence of abnormal corneal endothelium on the iris stroma and anterior chamber angle leading to usually unilateral, progressive iris atrophy, glaucoma, and/or corneal edema. The etiology is yet unclear. It affects mostly young adults, mostly females. Management of iridocorneal endothelial syndrome is complex: conservative and surgical, depending on the stage of the disease and intensity of present symptoms. A 30-year-old

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20

Suresh, Ruthra, and Samuel Cornelius Gnanadurai. "Rare case of iridocorneal endothelial syndrome with secondary glaucoma." Indian Journal of Clinical and Experimental Ophthalmology 8, no. 4 (2022): 563–66. http://dx.doi.org/10.18231/j.ijceo.2022.114.

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A rare case of 40 years old female, came with complaints of pain and blurring of vision in the left eye for the past week. The patient had a diminution of vision since birth in her left eye. On examination left eye vision was found to be 6/60 not improving with pinhole, also defective color vision 20/25. The right-eye vision was found to be normal. The left eye showed significant corneal edema, and moderate anterior chamber depth, with iris features of Corectopia, Pseudopolycoria, and iris atrophy. Pressures were found to be 30mm hg in the left eye, gonioscopy revealed high peripheral anterior

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21

Beganovic, Allen, Amra Vodencarevic, Meliha Halilbasic, and Anis Medjedovic. "Iridocorneal Endothelial Syndrome: Case Report of Essential Progressive Iris Atrophy." Medical Archives 76, no. 3 (2022): 224. http://dx.doi.org/10.5455/medarh.2022.76.224-228.

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Background: Iridocorneal endothelial (ICE) syndrome is a group of ophthalmic disorders, first reported by Eagle and Yanoff in 1979, a disease characterized by abnormalities of the iris and the corneal endothelium, and mainly occurs unilaterally in young and middle-aged women, with no family history. ICE syndrome comprises a spectrum of three clinical variants: Progressive essential iris atrophy (corectopia, iris atrophy or iris hole), Chandler syndrome (corneal oedema with mild to absent iris change), and Cogan - Reese syndrome (nodular pigmented lesion of the iris). Objective: We are presenti

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22

Markovic, Vujica, Aleksandra Radosavljevic, Dragan Vukovic, et al. "The frequency of secondary glaucoma in patients with iridocorneal endothelial syndrome in correlation to the presence of uveal ectropion." Srpski arhiv za celokupno lekarstvo 145, no. 5-6 (2017): 239–46. http://dx.doi.org/10.2298/sarh160526042m.

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Introduction/Objective. Iridocorneal endothelial (ICE) syndrome incudes 3 clinical forms: progressive iris atrophy, Chandler?s syndrome, and Cogan?Reese syndrome. It is characterized by various degrees of iris atrophy, corneal endothelial changes, uveal ectropion, corectopia, peripheral anterior synechiae (PAS) and secondary glaucoma. The aim of the study was to illustrate forms of ICE syndrome, determine frequency of secondary glaucoma with emphasis on cases with uveal ectropion, analyze response to medicament treatment and the need for surgical treatment in intraocular pressure (IOP) control

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23

Tasya Rahma, Fanni, Nasrudin Nasrudin, and Saskia Nassa Mokoginta. "Iridocorneal Endothelial Syndrome." Jurnal sosial dan sains 5, no. 3 (2025): 490–501. https://doi.org/10.59188/jurnalsosains.v5i3.31977.

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Salah satu gangguan endotel kornea yang langka terjadi adalah sindrom ICE yang merupakan kelompok penyakit yang ditandai dengan sel-sel endotel kornea abnormal pada stroma iris dan sudut bilik mata anterior. Etiologi sindrom ini belum jelas. Penanganan sindrom ini sulit dilakukan karena bersifat progresif. Melakukan diagnosis dan manajemen multidisiplin yang cepat dan tepat dapat meminimalisir risiko fatal. Laporan kasus ini bertujuan untuk menganilisis kasus seorang perempuan yang mengalami gangguan pada endotel kornea mata kanannya disertai dengan glaukoma primer sudut tertutup. Penelitian i

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24

Nutterová, Elena, Šárka Pitrová, and Ján Lešták. "Our Experience With Micropulse Cyclophotocoagulation in the Therapy Of Glaucoma." Czech and Slovak Ophthalmology 76, no. 1 (2020): 29–34. http://dx.doi.org/10.31348/2020/4.

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The objective of this study was a retrospective assessment of two-year experience with micropulse cyclophotocoagulation (MP CPC) in the therapy of various types of glaucoma. Material and method: The cohort of patients consisted of 47 people, out of which 16 men and 31 women. An average age of males was 58.9 years (the range from 35 to 78 years), and an average age of females was 64.7 years (the range from 33 to 86 years). Both eyes were treated in three patients, and therefore the total number of assessed eyes was 50. Patients who underwent the therapy were in different stages of glaucoma dise

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25

Daus, W., H. Völcker, M. Steinbrück, and F. Rentsch. "Zur Klinik und Histopathologie des Cogan-Reese-Syndroms." Klinische Monatsblätter für Augenheilkunde 197, no. 08 (1990): 150–55. http://dx.doi.org/10.1055/s-2008-1046259.

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26

Lago, Anelise de Medeiros, Ricardo Henrique Goulart Bittar, Larissa Rossana Souza Stival, and João Jorge Nassaralla Junior. "Cogan Reese syndrome." Revista Brasileira de Oftalmologia 75, no. 1 (2016). http://dx.doi.org/10.5935/0034-7280.20160013.

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27

Gupta, Kajree, Sushmita Kaushik, and Ashok Kumar Singh. "Easy Miss: Early Cogan Reese Syndrome." Ophthalmology Glaucoma, September 2022. http://dx.doi.org/10.1016/j.ogla.2022.08.008.

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28

Praveena, Guddeti. "Cogan- Reese Syndrome: A Variant of Iridocorneal Endothelial Syndrome." Delhi Journal of Ophthalmology 28, no. 4 (2018). http://dx.doi.org/10.7869/djo.366.

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29

Husnaini, Husnaini. "TRABEKULEKTOMI DENGAN MITOMYCIN-C PADA COGAN-REESE SYNDROME." Syifa' MEDIKA: Jurnal Kedokteran dan Kesehatan 10, no. 2 (2020). http://dx.doi.org/10.32502/sm.v10i2.2158.

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30

Karandikar, Sumita, Nilay Patel, and Nita Shanbhag. "Iridocorneal endothelial syndrome: iris naevus (Cogan-Reese) syndrome. A case report." International Journal of Research in Medical Sciences, 2015, 3420–23. http://dx.doi.org/10.18203/2320-6012.ijrms20151203.

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31

Alvaro, Tello Fernández, Mallén Gracia Víctor, Munuera Rufas Inés, Buil Martínez Mireia, García Hermosín Mario, and Marcén Solanas Elena. "IRIDOCORNEAL ENDOTHELIAL SYNDROME, TREATMENT ALTERNATIVES." Revista sanitaria de investigación IV, no. 03 (2023). http://dx.doi.org/10.34896/rsi.2023.15.83.001.

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El síndrome endotelial iridocorneal (SICE) incluye una serie de patologías (Síndrome de Chandler, Atrofia Progresiva de Iris y Síndrome de Cogan Reese) que afectan al segmento anterior del ojo caracterizadas por la proliferación de células endoteliales anómalas, cuya extensión en las estructuras angulares y corneales puede desembocar en edema corneal y glaucoma. Son habitualmente unilaterales y más frecuentes en mujeres jóvenes. La principal hipótesis que se baraja para la aparición de este tipo de células endoteliales anómalas es que existe una infección viral que desencadena su conversión, a

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