Search results for "Achromatopsia"

showing 9 items of 9 documents

Empirical mode decomposition and neural network for the classification of electroretinographic data

2013

The processing of biosignals is increasingly being utilized in ambulatory situations in order to extract significant signals' features that can help in clinical diagnosis. However, this task is hampered by the fact that biomedical signals exhibit a complex behaviour characterized by strong non-linear and non-stationary properties that cannot always be perceived by simple visual examination. New processing methods need be considered. In this context, we propose to apply a signal processing method, based on empirical mode decomposition and artificial neural networks, to analyse electroretinograms, i.e. the retinal response to a light flash, with the aim to detect and classify retinal diseases…

EngineeringAchromatopsiaBiomedical EngineeringContext (language use)Settore FIS/03 - Fisica Della MateriaHilbert–Huang transformRetinal DiseasesNight BlindnessElectroretinographyMyopiamedicineHumansComputer visionCongenital stationary night blindnessSignal processingArtificial neural networkbusiness.industryVisual examinationEye Diseases HereditaryGenetic Diseases X-LinkedSignal Processing Computer-AssistedPattern recognitionmedicine.diseaseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Computer Science Applicationselectroretinogram empirical mode decomposition artificial neural network Achromatopsia Congenital Stationary Night BlindnessClinical diagnosisNeural Networks ComputerArtificial intelligencebusinessMedical & Biological Engineering & Computing
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Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene

2019

Achromatopsia (ACHM) is a hereditary cone photoreceptor disorder characterized by the inability to discriminate colors, nystagmus, photophobia, and low-visual acuity. Six genes have been associated with this rare autosomal recessively inherited disease, including the GNAT2 gene encoding the catalytic α-subunit of the G-protein transducin which is expressed in the cone photoreceptor outer segment. Out of a cohort of 1,116 independent families diagnosed with a primary clinical diagnosis of ACHM, we identified 23 patients with ACHM from 19 independent families with likely causative mutations in GNAT2, representing 1.7% of our large ACHM cohort. In total 22 different potentially disease-causing…

AdultMaleAchromatopsiagenetic structuresAdolescentChild preschoolDNA Copy Number VariationsColor Vision DefectsBiologymedicine.disease_causeHeterotrimeric GTP-Binding Proteins/genetics03 medical and health sciencesExonGene duplicationGeneticsmedicineHumansGenetic Predisposition to DiseaseCopy-number variationColor Vision Defects/geneticsChildGenetics (clinical)030304 developmental biologyAgedGenetics0303 health sciencesGNAT2MutationSettore MED/30 - Malattie Apparato Visivo030305 genetics & heredityBreakpointInfantSequence Analysis DNAExonsMiddle Agedmedicine.diseaseHeterotrimeric GTP-Binding ProteinsPhotoreceptor outer segmenteye diseasesPedigreeSettore BIO/18 - GeneticaSequence Analysis DNA/methodsyoung adultFemalesense organsachromatopsia copy number variations GNAT2 mutations transducinmutation
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Ahromatopsijas izpausmju korekcija ar krāsainām kontaktlēcām

2017

MĒRĶIS: Novērtēt filtru kontaktlēcu (KL) pielietojumu ahromatopsijas simptomu korekcijai. METODE: Pētījumā piedalījās 8 dalībnieki (6 sievietes un 2 vīrieši) vecumā no 8 mēnešiem līdz 25 gadiem, periodā no 2012. līdz 2016.gadam. Pēc oftalmoloģiskās pārbaudes un ahromatopsijas noteikšanas, tika veikta speciālās krāsainās KL pielaikošanas procedūra. Pacientu atbildes tika noteiktas ar anketas palīdzību un noteikts apžilbšanas laiks ar un bez piedāvātām KL. SECINĀJUMI: filtru KL samazināja fotofobiju; apžilbšanas laiks kļuvis salīdzināms ar normālā redzes gadījumu; dalībnieki atzinīgi novērtē psiholoģiskos un sociālos ieguvumus ar izrakstītām filtru KL.

filtered contact lensesphotophobiaFizikaglareachromatopsialight
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An approach based on wavelet analysis for feature extraction in the electroretinogram

2011

Most biomedical signals are non-stationary. The knowledge of their frequency content and temporal distribution is then useful in a clinical context. The wavelet analysis is appropriate to achieve this task. The present paper uses this method to reveal hidden characteristics and anomalies of the human a-wave, an important component of the electroretinogram since it is a measure of the functional integrity of the photoreceptors. We here analyse the time–frequency features of the a-wave both in normal subjects and in patients affected by Achromatopsia, a pathology disturbing the functionality of the cones. The results indicate the presence of two or three stable frequencies that, in the pathol…

Electroretinogram a-Wave Photoreceptoral response Achromatopsia Wavelet analysisSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)
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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

2005

Contains fulltext : 47591.pdf (Publisher’s version ) (Closed access) Achromatopsia is a congenital, autosomal recessively inherited disorder characterized by a lack of color discrimination, low visual acuity (<0.2), photophobia, and nystagmus. Mutations in the genes for CNGA3, CNGB3, and GNAT2 have been associated with this disorder. Here, we analyzed the spectrum and prevalence of CNGB3 gene mutations in a cohort of 341 independent patients with achromatopsia. In 163 patients, CNGB3 mutations could be identified. A total of 105 achromats carried apparent homozygous mutations, 44 were compound (double) heterozygotes, and 14 patients had only a single mutant allele. The derived CNGB3 mutatio…

AchromatopsiaGenetics and epigenetic pathways of disease [NCMLS 6]genetic structuresGATED CATION CHANNELCNGB3 mutationsNonsense mutationMutantCyclic Nucleotide-Gated Cation ChannelsColor Vision DefectsGenes RecessiveLocus (genetics)Gene mutationBiologyTOTAL COLOURBLINDNESSIon ChannelsCLONINGDogscyclic nucleotide-gated channelGNAT2GeneticsmedicineLOCUSAnimalsHumansMissense mutationNeurosensory disorders [UMCN 3.3]ACHM3 locusDog DiseasesAlleleAllelesGenetics (clinical)Geneticstotal colorblindnessGNAT2PHOTORECEPTORSDYSTROPHYmedicine.diseaseCONE DEGENERATIONGENEeye diseasesPhenotypeEvaluation of complex medical interventions [NCEBP 2]MutationRetinal Cone Photoreceptor Cellssense organsachromatopsiarod monochromacyALPHA-SUBUNIThuman activities
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Wavelet analysis of human photoreceptoral response

2010

Feature detection of biomedical signals is crucial for deepening our knowledge of the physiological phenomena giving rise to them. To achieve this aim, even if many analytic approaches have been suggested only few are able to deal with signals whose features are time dependent, and to provide useful clinical information. In this work we use the wavelet analysis to extract peculiarities of the early response of the photoreceptoral human system, known as a-wave ERG-component. The analysis of the a-wave features is important since this component reflects the functional integrity of the two populations of photoreceptors, rods and cones whose activation dynamics are not well known. Moreover, in …

Congenital stationary night blindnessAchromatopsiagenetic structuresmedicine.diagnostic_testbusiness.industryWavelet analysis photoreceptoral response Achromatopsia Congenital Stationary Night Blindness.Wavelet transformFeature detection (nervous system)BiologyNeurophysiologymedicine.diseaseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Time–frequency analysisWaveletmedicineComputer visionsense organsArtificial intelligencebusinessNeuroscienceElectroretinography2010 3rd International Symposium on Applied Sciences in Biomedical and Communication Technologies (ISABEL 2010)
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A comparison among different techniques for human ERG signals processing and classification

2014

A comparison among different techniques for human ERG signals processing and classification ( Articles not published yet, but available online Article in press About articles in press (opens in a new window) ) Barraco, R.a, Persano Adorno, D.a , Brai, M.a, Tranchina, L.b a Dipartimento di Fisica e Chimica, Università di Palermo and CNISM, Viale delle Scienze, Ed. 18, I-90128 Palermo, Italy b Laboratorio di Fisica e Tecnologie Relative - UniNetLab, Università di Palermo, Viale delle Scienze, Ed. 18, I-90128 Palermo, Italy Abstract Feature detection in biomedical signals is crucial for deepening our knowledge about the involved physiological processes. To achieve this aim, many analytic appro…

Achromatopsiagenetic structuresComputer scienceBiophysicsGeneral Physics and AstronomyColor Vision DefectsPrincipal component analysiWavelet analysisPattern Recognition AutomatedWaveletRetinal pathologieElectroretinographymedicineHumansRadiology Nuclear Medicine and imagingComputer visionFeature detection (computer vision)Principal Component AnalysisSignal processingFourier Analysisbusiness.industryWavelet transformSignal Processing Computer-AssistedPattern recognitionGeneral Medicinemedicine.diseaseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)eye diseasesERG signalClinical diagnosisPrincipal component analysissense organsArtificial intelligencebusinessErgPhysica Medica
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Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia

2002

Achromatopsia is an autosomal recessively inherited visual disorder that is present from birth and that features the absence of color discrimination. We here report the identification of five independent families with achromatopsia that segregate protein-truncation mutations in the GNAT2 gene, located on chromosome 1p13. GNAT2 encodes the cone photoreceptor-specific alpha-subunit of transducin, a G-protein of the phototransduction cascade, which couples to the visual pigment(s). Our results demonstrate that GNAT2 is the third gene implicated in achromatopsia.

Achromatopsiagenetic structuresMolecular Sequence DataColor Vision DefectsBiologymedicine.disease_causeRetinal Cone Photoreceptor CellsReportGNAT2 geneGeneticsmedicineHumansGenetics(clinical)TransducinGeneGenetics (clinical)GeneticsGNAT2Mutationmedicine.diseaseRod monocromacyeye diseasesPedigreeColor Vision DefectsMutationRetinal Cone Photoreceptor CellsAchromatopsiaTransducinsense organsVisual phototransductionThe American Journal of Human Genetics
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A study of the human rod and cone electroretinogram a-wave component

2009

The study of the electrical response of the retina to a luminous stimulus is one of the main fields of research in ocular electrophysiology. The features of the first component (a-wave) of the retinal response reflect the functional integrity of the two populations of photoreceptors: rods and cones. We fit the a-wave for pathological subjects with functions that account for possible mechanisms governing the kinetics of the photoreceptors. The paper extends a previous analysis, carried out for normal subjects, in which both populations are active, to patients affected by two particular diseases that reduce the working populations to only one. The pathologies investigated are Achromatopsia, a…

Statistics and ProbabilityCongenital stationary night blindnessRetinaAchromatopsiagenetic structuresbusiness.industryStatistical and Nonlinear PhysicsRetinalBiologyStimulus (physiology)medicine.diseaseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)electroretinogram a-wavechemistry.chemical_compoundElectrophysiologyFunctional integrityOpticsmedicine.anatomical_structurechemistrymedicinesense organsStatistics Probability and UncertaintybusinessNeuroscienceVisual phototransduction
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