Kaitlin Kogachi, A. Ter-Zakarian, Jack J. Tian, R. Karanjia, A. Sadun
{"title":"The Elusive Pathophysiology of Leber's Hereditary Optic Neuropathy","authors":"Kaitlin Kogachi, A. Ter-Zakarian, Jack J. Tian, R. Karanjia, A. Sadun","doi":"10.15234/VPA.V15I4.352","DOIUrl":"https://doi.org/10.15234/VPA.V15I4.352","url":null,"abstract":"Leber’s Hereditary Optic Neuropathy (LHON) is a mitochondrially inherited disorder characterized by rapid, subacute vision loss. LHON has historically been a difficult disease to study due to its low incidence. Many questions concerning its pathophysiology have remained unanswered. A significant enigma concerns LHON’s gender bias as represented by the male-to-female ratio of about 4:1. Another source of confusion includes the variable penetrance, since the mitochondrial mutation is necessary, but not sufficient, to cause conversion. A third challenge involves the tissue specificity, since typically only the optic nerve is involved with a specific pattern of optic atrophy due to primary loss of the papillomacular bundle (PMB) in affected individuals. The fourth remaining complexity is the pattern of rapid, subacute vision loss observed in nearly all affected individuals. Several clinical genetic studies, cybrid experiments, and histochemical studies have been conducted to address the three enigmas of gender bias, variable penetrance, and tissue specificity. Despite elucidation of these three aspects of the pathophysiology, the mechanism behind the rapid, significant vision loss remains a mystery.","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"47 1","pages":"102-105"},"PeriodicalIF":0.0,"publicationDate":"2016-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76250834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jorge-Emmanuel Morales-León, Karla Dueñas-Ángeles, Celia Elizondo-Olascoaga, Curt Hartleben-Matkin
{"title":"Prevalence of angle closure disease in an ophthalmology teaching hospital before and after encouragement of gonioscopy","authors":"Jorge-Emmanuel Morales-León, Karla Dueñas-Ángeles, Celia Elizondo-Olascoaga, Curt Hartleben-Matkin","doi":"10.15234/VPA.V15I4.177","DOIUrl":"https://doi.org/10.15234/VPA.V15I4.177","url":null,"abstract":"Purpose To determine differences in prevalence of angle closure disease (ACD) in a glaucoma department of an ophthalmology teaching hospital before and after strategies promoting gonioscopy were implemented. To characterize patients with angle closure disease and also when divided by Foster classification in a heterogeneous Latin American population. Study design Retrospective, observational, case-control study. Material and methods We reviewed every electronic medical record from July 2010 and July 2013 from the glaucoma department at our institution. Prevalence was obtained from the diagnosis of electronic medical records and we characterized patients with general ACD and also when dividing them according to Foster ACD classification Results: We reviewed 2112 medical records from July 2010 and 2549 medical records from 2013. Angle closure disease prevalence went from 7.29% (n=154) in 2010 to 20.36% (n=519) in 2013. Prevalence of primary open angle glaucoma (POAG) decreased from 23.20% to 10.84% in the same period of time. Angle closure disease characterization revealed that women are the most affected gender Conclusions: Promoting the performance of a standardized and supervised gonioscopy to all patients of a glaucoma department in an ophthalmology teaching hospital, resulted in 1.79 times more diagnosis of angle closure compared to a time when it was not compulsory. Characterization showed that angle closure patients tend to be women, with decreasing low hyperopia and normal office intraocular pressures, especially when treated with antiglaucoma medications.","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"92 1","pages":"106-109"},"PeriodicalIF":0.0,"publicationDate":"2016-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76447942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rachel S. Mogil, S. Fragiotta, G. Barile, Jamie R Mitchell
{"title":"Acute Macular Neuroretinopathy Presenting as Bitemporal Defects on Humphrey Visual Field","authors":"Rachel S. Mogil, S. Fragiotta, G. Barile, Jamie R Mitchell","doi":"10.15234/VPA.V15I3.343","DOIUrl":"https://doi.org/10.15234/VPA.V15I3.343","url":null,"abstract":"A 25-year-old woman presented with blurry vision, headache, nausea, and syncope. Humphrey visual field testing revealed bitemporal defects, but magnetic resonance imaging was negative for chiasmal pathology. Macular optical coherence tomography showed focal parafoveal disruption of the photoreceptor inner segment/outer segment junction and infrared imaging showed hyporeflective macular lesions in both eyes. Our case demonstrates a diagnosis of acute macular neuroretinopathy that presented with bitemporal visual field defects. To our knowledge, bitemporal visual field loss, mimicking chiasmal pathology, has not been reported previously in association with acute macular neuroretinopathy.","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"56 4","pages":"92-94"},"PeriodicalIF":0.0,"publicationDate":"2016-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72549430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
N. Marques, A. Miranda, S. Barros, S. Parreira, N. Mejias, Belmira Belran, N. Campos, João Cardoso
{"title":"Posterior Scleritis and Myelodisplasia in Relapsing Polychondritis- Case Report and Literature Review","authors":"N. Marques, A. Miranda, S. Barros, S. Parreira, N. Mejias, Belmira Belran, N. Campos, João Cardoso","doi":"10.15234/VPA.V15I3.314","DOIUrl":"https://doi.org/10.15234/VPA.V15I3.314","url":null,"abstract":"Relapsing Polychondritis (RP) is a rare, recurrent and autoimmune multisytem disorder affecting cartilaginous structures, such as: auricles, joints, nasal septum, larynx and tracheobronchial tree. Ocular manifestations may appear in 42,3-65% of cases (1,2), episcleritis and scleritis being the most common. However, it is often presented in an enigmatic fashion and is misdiagnosed, leading to potentially severe, debilitating and, sometimes, fatal disease. There is no established standardized therapeutic protocol for RP. Current medical therapy is largely empiric and based on case reports. The aim of this paper is to document one more case of ocular involvement in RP disease emphasizing the clinical and imaging findings that can help to establish an early diagnosis. Keywords: Relapsing Polychondritis; Autoimmune disease; Myelodysplastic Syndrome; Scleritis/treatment; Case Reports","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"18 1","pages":"87-88"},"PeriodicalIF":0.0,"publicationDate":"2016-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90140733","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Review of Scleral Flap Shape on Trabeculectomy Outcomes","authors":"Megan A Rowlands, A. Maharaj","doi":"10.15234/VPA.V15I3.345","DOIUrl":"https://doi.org/10.15234/VPA.V15I3.345","url":null,"abstract":"Introduction : Trabeculectomies are amongst the most common surgical procedures to lower intraocular pressure (IOP). Scleral flap dimensions are a key factor in influencing aqueous outflow and subsequent IOP reduction, especially in the early postoperative period. Despite the substantial diversity of scleral flap shapes that is used in practice, there is little information comparing outcomes between them. In this study, we review the literature on the uses and outcomes of various scleral flap shapes. Methods: A literature review was performed using the databases: MEDLINE, SCOPUS, and Web of Science. Search terms for relevant studies included the following: trabeculectomy AND (square OR triang* OR rectang* OR polygon* OR arc OR shape) AND flap. Results: Our initial literature search revealed 71 unique articles, six of which met our inclusion and exclusion criteria and were reviewed. Four articles reported the use of triangular flaps, one rectangular flap, one square flap, and two arc-shaped flaps. The data from each article were reviewed for the following: Surgical technique Early postoperative intraocular pressure reduction Final postoperative intraocular pressure reduction Postoperative complications Conclusions: A myriad of scleral flap shapes is utilized in surgical practice. Essentially all of the trabeculectomy procedures, regardless of scleral flap shape, achieved substantial reductions in IOP with similar success rates. However, due to the variability in surgical technique and lack of direct comparison, we cannot definitively conclude or deny that one flap shape is superior to another. We believe our review provides the most comprehensive analysis of scleral flap shape to date and highlights its importance in regulating aqueous flow, especially in the early postoperative period.","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"1 1","pages":"70-74"},"PeriodicalIF":0.0,"publicationDate":"2016-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90414805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"OCULAR INJURIES CAUSED BY LIGHTNING STRIKES: REVIEW OF THE LITERATURE AND PRESENTATION OF TWO CLINICAL CASES","authors":"Jeanneth Toquica, H. Gómez","doi":"10.15234/vpa.v15i3.329","DOIUrl":"https://doi.org/10.15234/vpa.v15i3.329","url":null,"abstract":"Secondary injuries caused by lightning strikes are not frequent; however survivors have important sequelae in organs and tissues. We describe two cases, the first one with lightning-induced maculopathy and the other case involves lens damage. This paper discusses factors that determine the extent of injuries and review the management for each one.","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"5 1","pages":"84-86"},"PeriodicalIF":0.0,"publicationDate":"2016-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85489530","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Catarina Pedrosa, S. Pina, F. Paula, M. Amaral, F. Vaz
{"title":"Peripapillary retinal nerve fiber layer thickness and peripheral microcirculation in Raynaud's disease.","authors":"Catarina Pedrosa, S. Pina, F. Paula, M. Amaral, F. Vaz","doi":"10.15234/VPA.V15I3.324","DOIUrl":"https://doi.org/10.15234/VPA.V15I3.324","url":null,"abstract":"Introduction: Normal-tension glaucoma has been associated with systemic vascular diseases such as peripheral vasospasm. This study aims to evaluate the influence of peripheral vasospasm on the thickness of the retinal nerve fiber layer (RNFL) in Raynaud’s disease (RD), and the correlation between global RNFL and peripheral microcirculation features in RD patients. Methods: Observational cross-sectional study of 18 patients (35 eyes) with a diagnosis of RD followed in our clinic, and 20 healthy controls (39 eyes). RNFL parameters were obtained using spectral domain optical coherence tomography (SD-OCT Spectralisâ, Heidelberg). Global and sectorial peripapillary RNFL thickness were registered. Age, gender, refractive error, best-corrected visual acuity and intraocular pressure were determined, and slit-lamp biomicroscopy and fundus examination were performed. Nailfold videocapillaroscopy (NC) was performed in the RD group to characterize capillary morphology and blood flow. Mann-Whitney and Fisher’s exact tests were used for statistical analysis. Statistical significance level was set at p<0.05 (two-sided). Results: There was no significant difference in the global RNFL between RD patients and the control group (p=0.35). The presence of avascular areas in NC was associated with a lower global RNFL thickness (p=0.026). Conclusion: The association between avascular areas in NC and the lower global RNFL thickness in RD patients suggests that systemic vasospasm severity may be related to optic nerve lesion propensity. Therefore, its presence in NC may identify RD patients at risk for optic nerve head lesion. A larger sample with a long-term study is needed to support the clinical and therapeutic implications of our findings.","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"95 1","pages":"80-83"},"PeriodicalIF":0.0,"publicationDate":"2016-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83705750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"CURIOSITY MAKES YOU SMARTER","authors":"P. E. Dantas","doi":"10.15234/VPA.V15I2.348","DOIUrl":"https://doi.org/10.15234/VPA.V15I2.348","url":null,"abstract":"","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"21 1","pages":"35"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81493772","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"MESSAGE FROM THE PAAO PRESIDENT AND FROM THE CHAIRMAN OF THE PAOF BOARD","authors":"E. Alfonso","doi":"10.15234/VPA.V15I2.339","DOIUrl":"https://doi.org/10.15234/VPA.V15I2.339","url":null,"abstract":"","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"258 1","pages":"36"},"PeriodicalIF":0.0,"publicationDate":"2016-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76218840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Message from the Chairman of the Boardof the Board","authors":"L. Ventura","doi":"10.15234/vpa.v15i1.333","DOIUrl":"https://doi.org/10.15234/vpa.v15i1.333","url":null,"abstract":"","PeriodicalId":53032,"journal":{"name":"Vision PanAmerica","volume":"44 1","pages":"30"},"PeriodicalIF":0.0,"publicationDate":"2016-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81150235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}