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1.
Doc Ophthalmol ; 148(2): 75-85, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38488946

RESUMO

The pattern electroretinogram (PERG) is a localized retinal response evoked by a contrast-reversing pattern, usually a black and white checkerboard, which provides information about macular and retinal ganglion cell function. This document, from the International Society for Clinical Electrophysiology of Vision (ISCEV; www.iscev.org ) presents an updated and revised Standard for clinical PERG testing. This replaces the 2013 and all earlier versions. Minimum protocols for basic PERG stimuli, recording methods and reporting are specified, to promote consistency of methods for diagnosis and monitoring purposes, while responding to evolving clinical practices and technology. The main changes in the updated ISCEV Standard for clinical PERG include expanded guidance about large stimulus fields, stimulus parameters for simultaneous PERG and pattern visual evoked potential recording, baseline drift correction, and use of consistent ambient room lighting. These changes aim to provide a clinically relevant document about current practice which will facilitate good quality recordings and inter-laboratory comparisons.


Assuntos
Eletrorretinografia , Potenciais Evocados Visuais , Eletrorretinografia/métodos , Retina , Visão Ocular , Células Ganglionares da Retina
2.
Doc Ophthalmol ; 148(1): 3-14, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38238632

RESUMO

The full-field stimulus test (FST) is a psychophysical technique designed for the measurement of visual function in low vision. The method involves the use of a ganzfeld stimulator, as used in routine full-field electroretinography, to deliver full-field flashes of light. This guideline was developed jointly by the International Society for Clinical Electrophysiology of Vision (ISCEV) and Imaging and Perimetry Society (IPS) in order to provide technical information, promote consistency of testing and reporting, and encourage convergence of methods for FST. It is intended to aid practitioners and guide the formulation of FST protocols, with a view to future standardisation.


Assuntos
Eletrorretinografia , Testes de Campo Visual , Eletrorretinografia/métodos , Sociedades Médicas , Estimulação Luminosa/métodos , Visão Ocular
3.
BMJ Open Ophthalmol ; 8(Suppl 3): A3, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-37798009

RESUMO

Cerebral visual impairment (CVI) encompasses a heterogeneous group of disorders and a spectrum of types of visual impairments. Research is needed to characterise the different forms of CVI and identify the specific needs of these groups to inform individualised patient care. Homonymous hemianopia (HH) is a definable visual field defect that affect some children with CVI. As part of a new research programme, we conducted a scoping review of the literature on HH in children and young people to map current knowledge and identify evidence gaps.We used the PRISMA extension for Scoping Reviews methodology. Multiple online databases were searched using terms associated with 'homonymous hemianopia' and 'children'. This yielded 1588 papers which were screened by two reviewers. Of these 1001 were excluded at abstract screen and a further 415 excluded after full text review, with full text unavailable for 15. Data were extracted and charted from 157 studies and additional grey literature.Interim analysis shows reported studies are predominantly from high income countries with a paucity of higher-level evidence, and a preponderance of case reports. Most papers reported causative pathology and diagnosis of HH. There was minimal attention to or evidence relating to intervention. Child-specific grey literature on HH was limited.This review collates the current evidence-base for HH in children. It demonstrates the important evidence-gap relating to intervention in these cases that would help inform more individualised care. Similar scoping reviews may be prove useful in assessing the evidence relating to other definable groups within the CVI umbrella.


Assuntos
Encefalopatias , Hemianopsia , Humanos , Adolescente , Hemianopsia/diagnóstico , Testes de Campo Visual/efeitos adversos , Encefalopatias/complicações
4.
Eye (Lond) ; 37(6): 1178-1183, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-35562551

RESUMO

BACKGROUND/AIMS: Optic pathway gliomas (OPGs) may cause progressive visual loss despite chemotherapy. Newer, less toxic treatments might be given earlier, depending on visual prognosis. We aimed to investigate the prognostic value of visual evoked potentials (VEP) and optical coherence tomography (OCT). METHODS: A retrospective study of OPG patients (treated 2003-2017) was conducted. Primary outcome was PEDIG category visual acuity in better and worse eyes (good < = 0.2, moderate 0.3-0.6 and poor > = 0.7 logMAR). Binary logistic regression analysis was used to identify predictors of these outcomes. RESULTS: 60 patients (32 Neurofibromatosis type 1 [NF1] and 28 sporadic) had median presentation age 49 months (range 17-183) (NF1) and 27 months (range 4-92) (sporadic). Median follow up was 82 months (range 12-189 months). At follow up 24/32 (75%) of NF1 children and 14/28 (50%) of sporadic children had good better eye visual acuity and 11/32 (34%) of NF1 children and 15/28 (54%) of sporadics had poor worse eye acuity. Mean peripapillary retinal nerve fibre layer (RNFL) thickness predicted good better eye final acuity (OR 0.799, 95%CI 0.646-0.987, p = 0.038). Presenting with visual symptoms (OR 0.22 95% CI 0.001-0.508, p = 0.017) and poorer VEP scores (OR 2.35 95% CI 1.1-5.03, p = 0.027) predicted poor worse eye final acuity. 16 children had homonymous hemianopias at follow up, predicted by poor presenting binocular VEP score (OR 1.449 95%CI 1.052-1.995, p = 0.02). CONCLUSIONS: We found that both RNFL thickness on OCT and VEP were useful in predicting future visual acuity and vision and potentially in planning treatment. We had a high prevalence of homonymous hemianopia.


Assuntos
Neurofibromatose 1 , Glioma do Nervo Óptico , Criança , Humanos , Estudos Retrospectivos , Potenciais Evocados Visuais , Glioma do Nervo Óptico/diagnóstico , Neurofibromatose 1/diagnóstico , Retina , Tomografia de Coerência Óptica/métodos , Hemianopsia
8.
Br J Dermatol ; 184(1): 151-155, 2021 01.
Artigo em Inglês | MEDLINE | ID: mdl-32282055

RESUMO

BACKGROUND: Allergic contact dermatitis (ACD) to cosmetics is widely reported. To ensure we are accurately diagnosing ACD, patch test series should be continually reviewed to identify relevant and emerging allergens and highlight those that are outdated. The current British Society for Cutaneous Allergy (BSCA) facial series recommends 26 allergens and was last modified in 2012. OBJECTIVES: To review and update the BSCA facial series. METHODS: We retrospectively reviewed the results from 12 UK and Ireland patch test centres' facial series from January 2016 to December 2017. We recorded the number of allergens tested in each centre and the detection rate for each allergen. Using a 0·3% positive rate as the inclusion threshold, we established which allergens in the BSCA facial series had positive patch test rates < 0·3% and > 0·3%. Allergens not in the BSCA facial series that had a positive patch test rate > 0·3% were identified. RESULTS: Overall, 4224 patients were patch tested to the facial series. The number of allergens included in individual centres' facial series ranged from 24 to 66, with a total of 103 allergens tested across all centres. Twelve of the 26 allergens in the BSCA facial series had a positive patch test rate < 0·3% and 14 had a rate > 0·3%. Twenty-five allergens not recommended in the BSCA facial series had a positive patch test rate > 0·3%. CONCLUSIONS: This audit has highlighted the significant variation in practice that exists among patch test centres, despite a recommended facial series. The BSCA facial series has been updated and now contains 24 allergens. Fifteen allergens remain, 11 allergens have been dropped and nine new allergens have been added.


Assuntos
Dermatite Alérgica de Contato , Alérgenos/efeitos adversos , Dermatite Alérgica de Contato/diagnóstico , Dermatite Alérgica de Contato/etiologia , Humanos , Irlanda/epidemiologia , Testes do Emplastro , Estudos Retrospectivos
10.
Ultramicroscopy ; 209: 112858, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31884380

RESUMO

A strain characterization technique in a Scanning Transmission Electron Microscope (STEM) called "STEM Moiré GPA" (SMG) emerged recently as an efficient method to map the deformation field on large field of views (up to few microns in length scale). The technique is based on the interference between the scanning grid of the STEM electron probe and the periodic lattice of a crystalline material. The interference pattern (STEM Moiré hologram) is the result of an undersampling artifact, commonly named aliasing, occurring when less than two pixels are used to record a lattice spacing. The phase of the STEM Moiré fringes embeds the crystalline structure of the sample, and the variation of the phase can be related to a deformation field. To acquire a STEM Moiré hologram, the current practice is limited to choosing the periodicity of the scanning grid (pixel spacing) close to one lattice spacing. Such empirical recommendations are, however, insufficient since multiple lattice spacings are undersampled at once. The aliased spatial frequencies can overlap with each other in Fourier space making the STEM Moiré hologram not suitable for Geometric Phase Analysis (GPA) processing. In this study, a procedure is proposed to choose the optimal sampling parameters (pixel spacing and scanning rotation) for the STEM Moiré GPA application on any single crystal material. The procedure is then applied on a InP/InAs1-xPx/InP stack grown by Molecular Beam Epitaxy (MBE). Deformation profiles from different sampling conditions are compared to the established High-Resolution STEM GPA method, highlighting the reliability of the SMG method following the optimization process. The optimization protocol and the limits of SMG are finally discussed, and a generalization of the coherent sampling concept is proposed.

11.
Osteoporos Int ; 29(4): 953-960, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29429033

RESUMO

PURPOSE: Although half of women and one-quarter of men aged 50 and older will sustain an acute low-trauma fracture, less than a quarter receive appropriate secondary fracture prevention. The goal of this quality improvement demonstration project was to implement a Fracture Liaison Service (FLS) focused on secondary prevention of an osteoporotic fracture in three open health care systems aided by a cloud-based tool. METHODS: The pre-post study design examined the proportion of men and women over age 50 who received appropriate assessment (bone mineral density, vitamin D levels) and treatment (calcium/vitamin D, pharmacologic therapy) in the six months following a recently diagnosed fracture. The pre-study (Pre FLS) included a retrospective chart review for baseline data (N = 344 patients) within each health care system. In the post-evaluation (Post FLS, N = 148 patients), the FLS coordinator from each health care system examined these parameters following enrollment and for 6 months following the recently diagnosed fracture. Data were managed in the cloud-based FLS application tool. RESULTS: Ninety-three participants completed the program. The FLS program increased the percentage of patients receiving bone mineral density testing from 21% at baseline to 93% (p < 0.001) Post FLS implementation. Assessments of vitamin D levels increased from 25 to 84% (p < 0.001). Patients prescribed calcium/vitamin D increased from 36% at baseline to 93% (p < 0.001) and those prescribed pharmacologic treatment for osteoporosis increased on average from 20 to 54% (p < 0.001) Post FLS. CONCLUSIONS: We conclude that the FLS model of care in an open health care system, assisted by a cloud-based tool, significantly improved assessment and/or treatment of patients with a recently diagnosed osteoporotic fracture. Future studies are necessary to determine if this model of care is scalable and if such programs result in prevention of fractures. Mini-Abstract: The goal was to implement a Fracture Liaison Service (FLS) focused on secondary prevention of an osteoporotic fracture in open health care systems aided by a cloud-based tool. This model significantly improved assessment and/or treatment of patients with a recently diagnosed fracture.


Assuntos
Prestação Integrada de Cuidados de Saúde/organização & administração , Modelos Organizacionais , Fraturas por Osteoporose/prevenção & controle , Absorciometria de Fóton/métodos , Idoso , Densidade Óssea/fisiologia , Conservadores da Densidade Óssea/uso terapêutico , Cálcio/uso terapêutico , Computação em Nuvem , Suplementos Nutricionais , Uso de Medicamentos/estatística & dados numéricos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Osteoporose/diagnóstico , Osteoporose/tratamento farmacológico , Osteoporose/fisiopatologia , Fraturas por Osteoporose/fisiopatologia , Estudos Retrospectivos , Prevenção Secundária/organização & administração , Estados Unidos , Vitamina D/uso terapêutico
12.
Osteoporos Int ; 27(2): 683-90, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26286624

RESUMO

UNLABELLED: The aims of this study are to develop a cloud-based application of the Fracture Liaison Service for practitioners to coordinate the care of osteoporotic patients after suffering primary fractures and provide a performance feedback portal for practitioners to determine quality of care. The application provides continuity of care, improved patient outcomes, and reduced medical costs. INTRODUCTION: The purpose of this study is to describe the content development and functionality of a cloud-based application to broadly deploy the Fracture Liaison Service (FLS) to coordinate post-fracture care for osteoporotic patients. METHODS: The Bone Health Collaborative developed the FLS application in 2013 to support practitioners' access to information and management of patients and provide a feedback portal for practitioners to track their performance in providing quality care. A five-step protocol (identify, inform, initiate, investigate, and iterate) organized osteoporotic post-fracture care-related tasks and timelines for the application. A range of descriptive data about the patient, their medical condition, therapies and care, and current providers can be collected. Seven quality of care measures from the National Quality Forum, The Joint Commission, and the Centers for Medicare and Medicaid Services can be tracked through the application. RESULTS: There are five functional areas including home, tasks, measures, improvement, and data. The home, tasks, and data pages are used to enter patient information and coordinate care using the five-step protocol. Measures and improvement pages are used to enter quality measures and provide practitioners with continuous performance feedback. The application resides within a portal, running on a multitenant, private cloud-based Avedis enterprise registry platform. All data are encrypted in transit and users access the application using a password from any common web browser. CONCLUSION: The application could spread the FLS model of care across the US health care system, provide continuity of care, effectively manage osteoporotic patients, improve outcomes, and reduce medical costs.


Assuntos
Computação em Nuvem , Prestação Integrada de Cuidados de Saúde/organização & administração , Modelos Organizacionais , Fraturas por Osteoporose/prevenção & controle , Conservadores da Densidade Óssea/uso terapêutico , Protocolos Clínicos , Prestação Integrada de Cuidados de Saúde/normas , Humanos , Colaboração Intersetorial , Osteoporose/tratamento farmacológico , Prevenção Secundária/organização & administração , Prevenção Secundária/normas , Estados Unidos
13.
Eye (Lond) ; 29(7): 936-42, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25998941

RESUMO

AIMS: To report the clinical phenotype in a series of four children from three families with the rare association of high myopia, central macular atrophy, and normal full-field electroretinography (ERG). METHODS: Four male patients were ascertained with reduced vision, nystagmus, and atrophy of the macula from early childhood. Patients underwent full ophthalmic examination, electrophysiological testing, and retinal imaging. RESULTS: Minimum duration of follow-up was 8 years. At last review, visual acuity ranged from 0.22 to 1.20 logMAR (6/9.5-6/95 Snellen) at a mean age of 10.5 years (median 9.5 years, range 9-14 years). Refractive error ranged from a spherical equivalent of -7.40 D to -24.00 D. Three had convergent squint. Fundus examination and imaging demonstrated bilateral macular atrophy in all patients that varied from mild atrophy of the retinal pigment epithelium (RPE) to well-demarcated, punched-out atrophic lesions of retina, RPE, and choroid. Flash ERG was normal under photopic and scotopic conditions in all patients. Pattern ERG, performed in three patients, was consistent with mild to severe macular dysfunction. Progression of the area of atrophy was evident in one patient and of the myopia in two patients but all patients had stable visual acuity. CONCLUSIONS: Patients with congenital high myopia and macular atrophy present in infancy with reduced visual acuity and nystagmus. The macular atrophic lesions vary in size and severity but electrophysiological testing is consistent with dysfunction confined to the macula. There was no deterioration in visual acuity over 8-10 years of monitoring.


Assuntos
Distrofias Hereditárias da Córnea/diagnóstico , Miopia Degenerativa/diagnóstico , Nistagmo Patológico/diagnóstico , Adolescente , Criança , Eletrorretinografia , Angiofluoresceinografia , Seguimentos , Humanos , Masculino , Miopia Degenerativa/congênito , Fenótipo , Estimulação Luminosa , Retina/fisiologia , Irmãos , Transtornos da Visão/diagnóstico , Acuidade Visual/fisiologia , Campos Visuais
14.
Doc Ophthalmol ; 130(2): 83-101, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25720529

RESUMO

BACKGROUND: The reproducibility of an individual's full-field ERG between centres has not previously been investigated. METHODS: ERGs were recorded using both silver thread and skin electrodes from the same two normal adult subjects at 15 UK centres using routine, local protocols and a highly standardised, 'ISCEV-specified' protocol matching the values specified in the ISCEV standard; where the ISCEV standard allows options, a single value was chosen. RESULTS: Inter-ocular differences were small, and amplitudes were smaller for skin than silver thread electrodes. No centre produced outlying data points, and ERGs across all 15 centres were remarkably similar. Amplitude variability was less for local protocols (using LED flashes) than for the ISCEV-specified protocol using xenon flashes (22 vs. 24 %, p = 0.01), but peak time variability was less for the ISCEV-specified protocol (6.1 vs. 7.4 %, p = 0.001). Only the DA 0.01 ERG correlated with photometric variability. The bifidity of the DA 3 a-wave doubled its peak time variability compared with the DA 10 a-wave. CONCLUSIONS: Inter-centre amplitude variability was typically within clinically significant thresholds, suggesting that inter-centre variability with suitable standardisation may not add more to total variability than inter-subject variability. Variability improvements gained by the tighter specifications of the ISCEV-specified protocol were possibly more than lost due to imprecisions of xenon flashtubes. Peak time variability was far lower than amplitude variability, corresponding with acceptable variability of biochemical assays. These results represent a vindication of the existence of an ERG standard and suggest that further standardisation would lend itself to greater reproducibility of ERGs worldwide.


Assuntos
Eletrorretinografia/normas , Retina/fisiologia , Adulto , Feminino , Resposta Galvânica da Pele , Voluntários Saudáveis , Humanos , Masculino , Estimulação Luminosa/métodos , Reprodutibilidade dos Testes , Adulto Jovem
16.
Nanotechnology ; 21(13): 134007, 2010 Apr 02.
Artigo em Inglês | MEDLINE | ID: mdl-20208111

RESUMO

GaAs nanowire (NW)-based p-n photovoltaic devices, with two distinct p and n spatial distributions and where Te was the n-dopant, have been studied by impedance spectroscopy in the 10(3)-10(7) Hz frequency range and the - 1.5-1.5 V bias range. For a large n-core/p-shell overlap region within NWs in a coaxial geometry, the p-n junction properties (DC rectification and p-n depletion capacitance) are found to prevail. The impedance data at low bias for both NW devices show large frequency dispersions with relaxation frequencies that are compatible with carrier re-emission times from traps due to GaAs surface states. An increasing conductance with increasing frequency for low bias is observed, suggesting hopping transport through localized states. For large bias the conductance increases exponentially with bias and is frequency independent, indicating conduction through extended states in this regime.

17.
Nanotechnology ; 21(13): 134005, 2010 Apr 02.
Artigo em Inglês | MEDLINE | ID: mdl-20208114

RESUMO

A semiconductor optical amplifier is grown on an InAsP metamorphic substrate to extend the long wavelength accessibility of the amplifier. The amplifier is shown to produce gain at wavelength exceeding 1640 nm while containing large tensile strain in the quantum wells. Also a laser diode is fabricated from the same device structure.

18.
Int J Obes (Lond) ; 32 Suppl 7: S19-27, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19136986

RESUMO

Named originally for their effects on peripheral end organs, the melanocortin system controls a diverse set of physiological processes through a series of five G-protein-coupled receptors and several sets of small peptide ligands. The central melanocortin system plays an essential role in homeostatic regulation of body weight, in which two alternative ligands, alpha-melanocyte-stimulating hormone and agouti-related protein, stimulate and inhibit receptor signaling in several key brain regions that ultimately affect food intake and energy expenditure. Much of what we know about the relationship between central melanocortin signaling and body weight regulation stems from genetic studies. Comparative genomic studies indicate that melanocortin receptors used for controlling pigmentation and body weight regulation existed more than 500 million years ago in primitive vertebrates, but that fine-grained control of melanocortin receptors through neuropeptides and endogenous antagonists developed more recently. Recent studies based on dog coat-color genetics revealed a new class of melanocortin ligands, the beta-defensins, which reveal the potential for cross talk between the melanocortin and the immune systems.


Assuntos
Peso Corporal/fisiologia , Sistema Nervoso Central/fisiologia , Ingestão de Alimentos/fisiologia , Receptores de Melanocortina/fisiologia , Proteína Agouti Sinalizadora , Proteína Relacionada com Agouti/genética , Proteína Relacionada com Agouti/metabolismo , Animais , Peso Corporal/efeitos dos fármacos , Sistema Nervoso Central/metabolismo , Cães , Ingestão de Alimentos/genética , Homeostase/genética , Homeostase/fisiologia , Humanos , Ligantes , Melanocortinas/metabolismo , Pigmentação/genética , Receptores de Melanocortina/genética , Receptores de Melanocortina/metabolismo , alfa-MSH/metabolismo , beta-Defensinas/fisiologia
19.
J Perinatol ; 26(8): 463-70, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16775621

RESUMO

OBJECTIVE: To test the psychometric soundness of a teamwork climate survey in labor and delivery, examine differences in perceptions of teamwork, and provide benchmarking data. DESIGN: Cross-sectional survey of labor and delivery caregivers in 44 hospitals in diverse regions of the US, using the Safety Attitudes Questionnaire teamwork climate scale. RESULTS: The response rate was 72% (3382 of 4700). The teamwork climate scale had good internal reliability (overall alpha = 0.78). Teamwork climate scale factor structure was confirmed using multilevel confirmatory factor analyses (CFI = 0.95, TLI = 0.92, RMSEA = 0.12, SRMR(within) = 0.04, SRMR(between) = 0.09). Aggregation of individual-level responses to the L&D unit-level was supported by ICC (1) = 0.06 (P < 0.001), ICC (2) = 0.83 and mean r (wg(j)) = 0.83. ANOVA demonstrated differences between caregivers F (7, 3013) = 10.30, P < 0.001 and labor and delivery units, F (43, 1022) = 3.49, P < 0.001. Convergent validity of the scale scores was measured by correlations with external teamwork-related items: collaborative decision making (r = 0.780, P < 0.001), use of briefings (r = 0.496, P < 0.001) and perceived adequacy of staffing levels (r = 0.593, P < 0.001). CONCLUSION: We demonstrate a psychometrically sound teamwork climate scale, correlate it to external teamwork-related items, and provide labor and delivery teamwork benchmarks. Further teamwork climate research should explore the links to clinical and operational outcomes.


Assuntos
Cuidadores/psicologia , Comportamento Cooperativo , Salas de Parto , Parto Obstétrico , Trabalho de Parto , Corpo Clínico Hospitalar/psicologia , Percepção Social , Adulto , Atitude do Pessoal de Saúde , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Cultura Organizacional , Gravidez , Psicometria
20.
Br J Ophthalmol ; 89(10): 1311-7, 2005 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16170123

RESUMO

AIM: To describe the clinical spectrum of achiasmia, a congenital disorder of reduced relative decussation at the optic chiasm. METHODS: A retrospective case note and patient review of nine children (four boys). Achiasmia was defined by the combination of a characteristic asymmetry of the monocular visual evoked potential (VEP) response to flash and neuroimaging showing reduced chiasmal size. RESULTS: Three of the children had an associated skull base encephalocele with agenesis of the corpus callosum. In two patients achiasmia was associated with septo-optic dysplasia. Three patients had no neuroimaging abnormalities other than reduced chiasmal size and have no known pituitary dysfunction. One child had multiple physical deformities but the only brain imaging abnormality was reduced chiasmal size. CONCLUSIONS: Some children with disorders of midline central nervous system development, including septo-optic dysplasia and skull base encephaloceles, have congenitally reduced chiasmal decussation. Reduced relative decussation may co-exist with overall chiasmal hypoplasia. Children with an apparently isolated chiasmal decussation deficit may have other subtle neurological findings, but our clinical impression is that most of these children function well.


Assuntos
Anormalidades Múltiplas , Quiasma Óptico/anormalidades , Adolescente , Agenesia do Corpo Caloso , Criança , Pré-Escolar , Encefalocele/fisiopatologia , Potenciais Evocados Visuais , Movimentos Oculares , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Quiasma Óptico/patologia , Estudos Retrospectivos , Base do Crânio/anormalidades , Acuidade Visual , Campos Visuais
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