Abstract Background This case report describes two rare cases of Coats disease in nonjuvenile patients with preserved vision. Case presentation Two otherwise healthy Asian males aged 15 and 29 years old presented with unilateral gradual blurred vision and scotoma, respectively. Visual acuity was 6/6 (0 logMAR) with no other abnormalities observed in the anterior segment of the eyes. Both posterior segment examinations and fluorescein angiography revealed retinal telangiectatic vessels, exudation, and hemorrhage. Additionally, optical coherence tomography of the first patient showed subfoveal fluid. Both patients were diagnosed with stage 2 Coats disease. Laser photocoagulation was performed on both patients. The first patient showed initial...
Background: In this article we share our experience of treating various severities of Coats' disease...
Purpose: To present a case of linear scleroderma known as “en coup de sabre” associated with Coats'-...
Purpose: We present the case of an 18-year-old Caucasian male with a unilateral macular star and ret...
Purpose. We describe an atypical case of a patient with Coats disease that re-emerged after 30 years...
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remi...
AbstractPurposeThe aim of this report was to demonstrate a case of Coats disease in a patient with c...
Tatsuro Otani1, Kanako Yasuda1, Naoko Aizawa2, Fumiaki Sakai3, Toru Nakazawa2, Masahiko Shimura11Dep...
Purpose. To describe the clinical response of refractory macular edema associated with Coats’ diseas...
Purpose: To evaluate the rarity, clinical features and management of Coats disease characterized by ...
Coats' disease is a nonhereditary ocular disease, with no systemic manifestation, first described by...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...
Yusoff Munira,1 Embong Zunaina,1,2 Yaakub Azhany1,2 1Department of Ophthalmology, School of Medical ...
To describe the clinical features of cataract during the course of Coats disease and to determine it...
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, c...
Coats' disease is characterized by retinal vascular telangiectasia and subretinal and intraretinal e...
Background: In this article we share our experience of treating various severities of Coats' disease...
Purpose: To present a case of linear scleroderma known as “en coup de sabre” associated with Coats'-...
Purpose: We present the case of an 18-year-old Caucasian male with a unilateral macular star and ret...
Purpose. We describe an atypical case of a patient with Coats disease that re-emerged after 30 years...
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remi...
AbstractPurposeThe aim of this report was to demonstrate a case of Coats disease in a patient with c...
Tatsuro Otani1, Kanako Yasuda1, Naoko Aizawa2, Fumiaki Sakai3, Toru Nakazawa2, Masahiko Shimura11Dep...
Purpose. To describe the clinical response of refractory macular edema associated with Coats’ diseas...
Purpose: To evaluate the rarity, clinical features and management of Coats disease characterized by ...
Coats' disease is a nonhereditary ocular disease, with no systemic manifestation, first described by...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...
Yusoff Munira,1 Embong Zunaina,1,2 Yaakub Azhany1,2 1Department of Ophthalmology, School of Medical ...
To describe the clinical features of cataract during the course of Coats disease and to determine it...
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, c...
Coats' disease is characterized by retinal vascular telangiectasia and subretinal and intraretinal e...
Background: In this article we share our experience of treating various severities of Coats' disease...
Purpose: To present a case of linear scleroderma known as “en coup de sabre” associated with Coats'-...
Purpose: We present the case of an 18-year-old Caucasian male with a unilateral macular star and ret...