Aims: To describe a Stargardt disease, (STGD1) is an autosomal recessive inherited disease often associated with mutations in ABCA4 and characterized by the accumulation of autofluorescent lipofuscin deposits in the retinal pigment epithelium (RPE). Presentation of Case: J.A.D.L...
Open access
Research Article10.9734/or/2021/v15i430219
Thiago Sande Miguel, Fernanda Bekman Diniz Mitleg Rocha, Tais Cristina Rossett, Felipe Bekman Diniz Mitleg Rocha, Eduardo de França Damasceno & Daniel Almeida da Costa·Ophthalmology Research: An International Journal·2022
Aims: To describe Congenital Ocular Melanocytosis. Presentation of Case: LPC, 7 years old, male, brown, with no previous comorbidities, was taken to the ophthalmology outpatient clinic of the Hospital Universitário Antônio Pedro, Brazil by parents who alleged the presence of blui...
Open access
Research Article10.9734/or/2022/v16i230231
Thiago Sande Miguel, Ana Luiza Mansur Souto, Fernanda Bekman Diniz Mitleg Rocha, Tais Cristina Rossett, Felipe Bekman Diniz Mitleg Rocha, Eduardo de França Damasceno & Daniel Almeida da Costa·Ophthalmology Research: An International Journal·2021
Aims: To describe a solar retinopathy. Presentation of Case: ALPN, 29 years old, male, with cognitive deficit that started after a car accident that occurred at the age of 6 years, attends the ophthalmology clinic of the University Hospital Antônio Pedro, Rio de Janeiro, Brazil w...
Open access
Research Article10.9734/or/2021/v15i230210