Search results for "Language disorder"

showing 10 items of 61 documents

Processing Past Tense in the left cerebellum

2014

We report the case of a patient with ischemic lesion of the left cerebellum, who showed specific deficits in processing past versus future tense of action verbs. These findings confirm, in the presence of cerebellar damage, previous results obtained with transcranial magnetic stimulation in healthy subjects and suggest a specificity of the left cerebellum for preparation of responses to the past tense of action verbs. As part of the procedural brain, the cerebellum could play a role in applying the linguistic rules for selection of morphemes typical of past and future tense formation.

MalefutureCerebellumcerebellummedicine.medical_treatmentNeuropsychological TestsPast tenseFunctional LateralityDevelopmental psychologyBrain IschemiaArts and Humanities (miscellaneous)MorphememedicineIschemic lesionReaction TimeverbsHumanspasttimeLanguage DisorderslanguageSettore M-PSI/02 - Psicobiologia E Psicologia FisiologicaHealthy subjectscerebellum; future; language; past; time; verbs; Brain Ischemia; Cerebellum; Functional Laterality; Humans; Language Disorders; Male; Middle Aged; Neuropsychological Tests; Reaction Time; LinguisticsLinguisticsMiddle AgedFuture tenseTranscranial magnetic stimulationmedicine.anatomical_structurenervous systemSettore MED/26 - NeurologiaNeurology (clinical)PsychologyNeuroscience
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Left minineglect or inverse pseudoneglect in children with dyslexia?

2011

International audience; This study compared the visuospatial asymmetries in children with dyslexia and healthy children by using the manual line bisection task, and investigated the processing of spatial context with a 'local' cueing paradigm consisting of geometric symbols placed on the extremities of the lines. The performance between healthy children (leftward bias) and children with dyslexia (rightward bias) was significantly different. Furthermore, the bisection mark was shifted in the direction of the unilaterally cued extremities in all children. As children with dyslexia showed a rightward bias in their spatial representation, which did not interfere with local context processing, w…

Malemedicine.medical_specialtyAdolescentBisectionmedia_common.quotation_subjectContext (language use)AudiologyNeuropsychological TestsDevelopmental psychologyNeglectDyslexiaPerceptual DisordersCommunication disordermedicineHumansLanguage disorderAttentionChildmedia_commonCued speechGeneral Neuroscience[SCCO.NEUR]Cognitive science/NeuroscienceDyslexiaCognitionmedicine.diseaseSpace Perception[ SCCO.NEUR ] Cognitive science/NeuroscienceFemalePsychologyPsychomotor PerformanceNeuroreport
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Event-related potentials in newborns with and without familial risk for dyslexia: principal component analysis reveals differences between the groups

2003

Differences revealed by factor scores extracted by principal component analysis (PCA) from event-related potential (ERP) data of newborns with and without familial risk for dyslexia were examined and compared to results obtained by using original averaged ERPs. ERPs to consonant-vowel syllables (synthetic /ba/, /da/, /ga/; and natural /paa/, /taa/, /kaa/) were recorded from 26 at-risk and 23 control 1-7 day-old infants. The stimuli were presented equiprobably and with interstimulus intervals varying at random from 3,910 to 7,285 ms. Statistically significant between-group differences were found to be relatively similar irrespective of the methods of analysis (original ERPs vs. factor scores…

Malemedicine.medical_specialtyAudiologyStimulus (physiology)behavioral disciplines and activitiesFunctional LateralityDevelopmental psychologyDyslexiaText miningPredictive Value of TestsEvent-related potentialCommunication disorderReaction TimemedicineHumansGenetic Predisposition to DiseaseLanguage disorderEvoked PotentialsBiological PsychiatryFamily HealthAnalysis of VariancePrincipal Component AnalysisLanguage TestsVerbal Behaviorbusiness.industryInfant NewbornDyslexiaBrainGenetic VariationReproducibility of ResultsElectroencephalographyFamilial riskmedicine.diseasePsychiatry and Mental healthAcoustic StimulationNeurologyPrincipal component analysisEvoked Potentials AuditoryFemaleNeurology (clinical)PsychologybusinessJournal of Neural Transmission
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Manifestation of speech and language disorders in children with hearing impairment compared with children with specific language disorders.

2010

Children with hearing impairment (HI) often suffer from speech and language disorders. We wondered if the manifestation of these disorders resembled the ones in children with specific language impairment (SLI). Using matched pairs, we compared the manifestation of a speech and language disorder in 5- and 6-year-old children with HI and SLI. We looked at receptive language skills using the Reynell scales, the lexicon, syntax and morphology, output phonology, and phonological short-term memory. Receptive language skills were more impaired in HI children. No significant differences were recorded for all other domains. We conclude that language deficits that are at least partially caused by the…

Malemedicine.medical_specialtyHearing lossHearing Loss SensorineuralMatched-Pair AnalysisSpecific language impairmentAudiologyLexiconbehavioral disciplines and activitiesSpeech DisordersHearing Loss BilateralSpeech and HearingArts and Humanities (miscellaneous)medicineHumansSpeechLanguage disorderCorrection of Hearing ImpairmentChildLanguage DisordersSyntax (programming languages)medicine.diagnostic_testPhonologyLPN and LVNmedicine.diseaseLanguage developmentMemory Short-TermPersons With Hearing ImpairmentsChild PreschoolAudiometry Pure-ToneFemalemedicine.symptomAudiometryPsychologyAudiometry SpeechChild LanguageLogopedics, phoniatrics, vocology
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Diagnostic subgroups of developmental dyslexia have different deficits in neural processing of tones and phonemes.

2004

The present study addressed auditory processing in 8-11-year-old children with developmental dyslexia by means of event-related brain potentials (ERP). Cortical sound reception was evaluated by recording N250 responses to syllables and tones and cortical sound discrimination by analyzing the mismatch negativity (MMN) to syllable and tone changes. We found that both cortical sound reception and sound discrimination were impaired in dyslexic children. The analysis of the data obtained from two dyslexic subgroups, Dyslexics-1 being impaired in non-word reading (or both non-word and frequent word reading) and Dyslexics-2 in frequent word reading but not in non-word reading, revealed that the MM…

Malemedicine.medical_specialtyMismatch negativityAudiologyElectroencephalography050105 experimental psychologyDevelopmental psychologyDyslexia03 medical and health sciences0302 clinical medicineCommunication disorderEvent-related potentialPhysiology (medical)medicineHumans0501 psychology and cognitive sciencesLanguage disorderChildmedicine.diagnostic_testGeneral Neuroscience05 social sciencesDyslexiaElectroencephalographymedicine.diseaseNeuropsychology and Physiological PsychologyAcoustic StimulationReadingAuditory PerceptionEvoked Potentials AuditorySpeech PerceptionFemaleSyllableAuditory PhysiologyPsychology030217 neurology & neurosurgeryInternational journal of psychophysiology : official journal of the International Organization of Psychophysiology
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Event-related potentials to pitch and rise time change in children with reading disabilities and typically reading children.

2008

Abstract Objective The purpose of the present study was to investigate whether children with reading disabilities (RD) process rise time and pitch changes differently to control children as a function of the interval between two tones. Methods Children participated in passive oddball event-related potential (ERP) measurements using paired stimuli. Mismatch negativity (MMN), P3a and late discriminative negativity (LDN) responses to rise time and pitch changes were examined. Results Control children produced larger responses than children with RD to pitch change in the P3a component but only when the sounds in the pair were close to each other. Compared to children with RD, MMN was smaller an…

Malemedicine.medical_specialtyTime FactorsMismatch negativityContingent Negative VariationAudiologyNeuropsychological TestsDevelopmental psychologyDyslexiaPitch DiscriminationP3aCommunication disorderEvent-related potentialPhysiology (medical)medicineReaction TimeHumansLanguage disorderChildBrain MappingDyslexiaElectroencephalographymedicine.diseaseSensory SystemsInterval (music)NeurologyAcoustic StimulationReadingRise timeMultivariate AnalysisEvoked Potentials AuditoryFemalesense organsNeurology (clinical)Psychologypsychological phenomena and processesClinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
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Static postural control in children with developmental dyslexia

2006

Correspondence to: Service d’Ophtalmologie, CHU de Dijon, 3 rue du Faubourg Raines, F-21000 Dijon, France. Tel.: +33 3 80 24 68 74; fax: +33 3 80 24 11 39.; International audience; The present investigation tries to better understand potential association and causal relationship between phonological and postural impairment due to developmental dyslexia. The study included 50 boys with developmental dyslexia and selected on the basis of their overall reading difficulties, and 42 control boys. Body sway during a quite standing posture eye open and eye closed on a force platform were tested in the two groups of subjects that were between 10 and 13 years of age. Analysis of classical parameters…

Malemedicine.medical_specialtyvisionstanding postureAdolescentmedia_common.quotation_subjectPosture[SHS.PSY]Humanities and Social Sciences/PsychologyAudiologyDevelopmental psychologyDyslexia[ SHS.PSY ] Humanities and Social Sciences/PsychologychildrenCommunication disorderReading (process)medicinePostural BalanceHumansForce platformLanguage disorderAssociation (psychology)ChildPostural Balancemedia_commonstabilometryGeneral NeuroscienceDyslexiaMotor controlmedicine.diseasedevelopmental dyslexiaPsychology
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Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment

2020

The 15q13.3 microdeletion (microdel15q13.3) syndrome (OMIM 612001) has been reported in healthy subjects as well as in individuals with a wide spectrum of clinical manifestations ranging from mild to severe neurological disorders, including developmental delay/intellectual disability, autism spectrum disorder, schizophrenia, epilepsy, behavioral problems and speech dysfunction. This study explored the link between this genomic rearrangement and nocturnal frontal lobe epilepsy (NFLE), which could improve the clinical interpretation. A clinical and genomic investigation was carried out on an 8-year-girl with a de novo deletion flanking the breakpoints (BPs) 4 and 5 of 15q13.3 detected by arra…

Migraine disorders.HypertrichosisPediatricsmedicine.medical_specialtyfrontal lobe epilepsyCase Report050105 experimental psychology03 medical and health sciencesEpilepsy0302 clinical medicinemigraine disorderslanguage disordersIntellectual disabilityMedicine0501 psychology and cognitive scienceschromosome breakpointsChromosome breakpointbusiness.industry05 social sciencesHypertrichosiLanguage disordermedicine.diseaseMigraine with aurahypertrichosisMigraineAutism spectrum disorderSchizophreniamedicine.symptombusinessLiterature surveychromosome breakpoints; frontal lobe epilepsy; hypertrichosis; language disorders; migraine disorders030217 neurology & neurosurgery
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FOXP2 polymorphisms in patients with schizophrenia.

2005

Abstract Background FOXP2 was described as the first gene involved in our ability to acquire spoken language. The main objective of this study was to compare the distribution of FOXP2 gene polymorphisms between patients with schizophrenia and healthy controls. Methods Two FOXP2 polymorphisms, Intron3a and SNP 923875, and the G→A transition in exon 14 were analysed in 149 patients with schizophrenia and schizoaffective disorders according to DSM-IV, as well as in 137 controls. All the patients showed a history of auditory hallucinations. Results The transition G→A at exon 14, detected in all the affected members in KE family, was not found in any of the analyzed samples from patients or cont…

OncologyAdultMalemedicine.medical_specialtyPsychosisGenotypeHallucinationsSeverity of Illness IndexExonPolymorphism (computer science)Internal medicinemedicineSNPHumansGenetic Predisposition to DiseaseAlleleBiological PsychiatryAllelesAgedDNA PrimersRetrospective StudiesGeneticsLanguage DisordersFOXP2 GenePolymorphism GeneticTransition (genetics)business.industryForkhead Transcription FactorsExonsMiddle Agedmedicine.diseaseIntronsDiagnostic and Statistical Manual of Mental DisordersPsychiatry and Mental healthSchizophreniaSchizophreniaFemalebusinessTranscription FactorsSchizophrenia research
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Slowly progressive aphasia: a four-year follow-up study

2001

This paper reports the long-term follow-up of GC, a patient with primary progressive aphasia of the fluent type. GC presented at onset with an anomia characterized by sparing of first letter knowledge, that applied mainly to proper names and living categories. No semantic deficits were observed in the first stage of the disease, and MRI showed a left temporal lobe atrophy with a gradient from the pole to the posterior regions, the latter being less involved. We now report the clinical evolution of GC from the 2nd to the 4th year of disease. As the disease progressed, the anomia became more severe and the phenomenon of first letter sparing was no longer detectable. Also semantic knowledge wa…

Pediatricsmedicine.medical_specialtyCognitive NeuroscienceSemantic dementiaExperimental and Cognitive PsychologyNeurological disorderNeuropsychological TestsTemporal lobePrimary progressive aphasiaBehavioral NeuroscienceAtrophyAphasiamedicineHumansSemantic memoryLanguage disorderMiddle Agedmedicine.diseaseSemanticsAphasia Primary ProgressiveDisease ProgressionFemalemedicine.symptomCognition DisordersPsychologyNeuroscienceFollow-Up StudiesNeuropsychologia
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