OBJETIVO: Analisar os achados clínico-oftalmológicos de portadores de nevo de Ota. MÉTODOS: Análise retrospectiva dos prontuários de pacientes com nevo de Ota. Foram registrados dados demográficos, localização do nevo e época do seu aparecimento, história familiar de manchas similares, olho acometido, achados ectoscópicos (classificação de Tanino), biomicroscópicos, fundoscópicos e campimétricos. RESULTADOS: Foram incluídos 14 pacientes, seis (47,0%) homens e oito (53,0%) mulheres com média de idade de 21,7±17,5 anos. Dez (71%) pacientes eram feodérmicos, três (21,4%) leucodérmicos e um (7,1%) […]

PURPOSE: To evaluate the retinal nerve fiber layer (RNFL) in sickle cell disease with optical coherence tomography (OCT). METHODS:The present study selected patients with sickle cell disease (SS) from the Federal University of Goias, and normalvolunteers, controlled by age and sex. Inclusion criteria for both groups were: visual acuity e” 20/30 without correction, intraocular pressure d” 21mmHg and a reliable and normal 24-2 Sita Standard visual field and optic disc. Thereafter, all subjects were submitted to OCT, Fast RNFL strategy, […]

The Ectopia lentis et pupillae is a rare genetic syndrome, congenital, autosomal recessive with variable expression, characterized by ectopia of the lens and the pupil, usually bilateral and symmetrical, but without systemic manifestations. The pathogenesis of this anomaly is still unknown, but there are theories that the change is mesodermal, neuroectodermal, combined or mechanical. This article presents a clinical case of a patient with ectopia lentis et pupillae, describing its clinical and genetic aspects, secondary ocular complications and differential diagnosis.

The aim of this report is to describe a case of iridocornel endothelial syndrome with the clinical variant essential iris atrophy, which presents concomitant congenital hypertrophy of the retinal pigment epithelium in the same eye.

The Sturge-Weber syndrome (SWS) is a rare congenital neuro-oculocutaneous disorder. This phacomatosis, also known as encephalotrigeminal angiomatosis, is defined by the classic triad: cutaneous, meningeal and ocular hemangiomas. Despite its typical presentation, incomplete forms are not uncommon. Glaucoma is often present and their pathophysiological mechanisms remain uncertain. Pherhaps this is why the clinical and surgical management of glaucoma associated with Sturge-Weber syndrome (GSSW) is a challenge for the ophthalmic practice, often with disappointing results. We present a literature review with […]

OBJECTIVE: To relate the efficacy of Molteno third generation glaucoma implant in four glaucoma patients. METHODS: Four glaucoma patients were submitted to Molteno third generation glaucoma implant. We evaluated intraocular pressure (IOP), visual acuity (VA), biomicroscopy exam and complications until six months after surgery. RESULTS: During six months we evaluated four glaucoma patients submitted to Molteno third generation glaucoma implant. Two cases had total success, one case had relative success and one case we had to take out the implant […]

PURPOSE: To evaluate the indications and results after penetrating keratoplasty in children at Altino Ventura Foundation (FAV). METHODS: A retrospective study was performed in 33 patients (34 eyes), with ages equal or less than 12 years, they underwent a penetrating keratoplasty at FAV, from 2000 to 2009. The mean follow up time was 32.5 ± 23.1 months. Surgery indication, best corrected visual acuity (BCVA) before and after surgery, spherical equivalent (SE) pos surgical and complications were analyzed. The qualitative results […]

Fuchs’ heterochromic iridocyclits or Fuchs’ Syndrome is a kind of uveitides relatively uncommon. Affect equally both genders, between 20-45 years old, in the classic features include a chronic unilateral nongranulomatous inflammation in anterior uvea, insidious onset, low-grade in activity, and unresponsive to corticosteroid therapy. Usually has a good prognosis, except for the development of cataract and glaucoma, pathologies associated with syndrome. In this case, there are a male pacient, 68 years, with glaucoma as the first manifestation of the Fuchs’Syndrome.