Search results for "development disorders"

showing 10 items of 54 documents

Left hemisphere enhancement of auditory activation in language impaired children

2019

| openaire: EC/H2020/641652/EU//ChildBrain Specific language impairment (SLI) is a developmental disorder linked to deficient auditory processing. In this magnetoencephalography (MEG) study we investigated a specific prolonged auditory response (N250m) that has been reported predominantly in children and is associated with level of language skills. We recorded auditory responses evoked by sine-wave tones presented alternately to the right and left ear of 9–10-year-old children with SLI (n = 10) and children with typical language development (n = 10). Source analysis was used to isolate the N250m response in the left and right hemisphere. In children with language impairment left-hemisphere …

0301 basic medicineMaleneurofysiologialcsh:MedicineSpecific language impairmentAudiologyBrain mapping3124 Neurology and psychiatryActivation pattern0302 clinical medicinesensory processinglcsh:Science10. No inequalityChildspecific language impartmentpathophysiologyBrain MappingMultidisciplinarymedicine.diagnostic_testBrainkuuloLanguage developmentAuditory PerceptionEvoked Potentials AuditorySensory processingFemalePsychologyAuditory perceptionauditory responsemedicine.medical_specialtyauditory evoked potentialModels Neurologicaldevelopmental language disorderNeurophysiologyLateralization of brain functionArticle03 medical and health sciencesmedicineHumansLanguage Development Disordershumankielellinen erityisvaikeuslcsh:RMagnetoencephalographybiological modelmedicine.diseaseDevelopmental disorder030104 developmental biologyhearinglcsh:Q030217 neurology & neurosurgeryScientific Reports
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Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four‐member family and an unrelated boy

2020

Abstract Background Deletions in chromosome 15q13 have been reported both in healthy people and individuals with a wide range of behavioral and neuropsychiatric disturbances. Six main breakpoint (BP) subregions (BP1‐BP6) are mapped to the 15q13 region and three further embedded BP regions (BP3‐BP5). The deletion at BP4‐BP5 is the rearrangement most frequently observed compared to other known deletions in BP3‐BP5 and BP3‐BP4 regions. Deletions of each of these three regions have previously been implicated in a variable range of clinical phenotypes, including minor dysmorphism, developmental delay/intellectual disability, epilepsy, autism spectrum disorders, behavioral disturbances, and speec…

AdultMale0301 basic medicinespeech delayAdolescentlcsh:QH426-470BP3-BP5 deletionspeech delay.Chromosome DisordersLocus (genetics)030105 genetics & heredity03 medical and health sciencesEpilepsySettore MED/38 - Pediatria Generale E SpecialisticaSeizuresIntellectual DisabilityIntellectual disabilitychromosome 15 q13GeneticsmedicineHumansLanguage Development DisordersChildMolecular BiologyGenetics (clinical)GeneticsChromosomes Human Pair 15business.industryBreakpointlanguage impairmentOriginal Articlesmedicine.diseasePhenotypePedigreeBP3‐BP5 deletiondevelopmental delayLanguage developmentlcsh:GeneticsPhenotype030104 developmental biologyBP3-BP5 deletion; chromosome 15 q13; developmental delay; language impairment; speech delaySpeech delayAutismFemaleOriginal ArticleChromosome Deletionmedicine.symptombusinessMolecular Genetics & Genomic Medicine
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Infant information processing and family history of specific language impairment: converging evidence for RAP deficits from two paradigms

2007

An infant's ability to process auditory signals presented in rapid succession (i.e. rapid auditory processing abilities [RAP]) has been shown to predict differences in language outcomes in toddlers and preschool children. Early deficits in RAP abilities may serve as a behavioral marker for language-based learning disabilities. The purpose of this study is to determine if performance on infant information processing measures designed to tap RAP and global processing skills differ as a function of family history of specific language impairment (SLI) and/or the particular demand characteristics of the paradigm used. Seventeen 6- to 9-month-old infants from families with a history of specific l…

AdultMaleCognitive NeuroscienceSpecific language impairmentLanguage DevelopmentArticleDevelopmental psychologyDevelopmental and Educational PsychologymedicineHumansLanguage Development DisordersCognitive skillHabituationHabituation PsychophysiologicRecognition memoryFamily HealthLanguage TestsNew JerseyAuditory Perceptual DisordersAge FactorsNoveltyInfantRecognition PsychologyCognitionmedicine.diseaseLanguage acquisitionLanguage developmentAcoustic StimulationCase-Control StudiesAuditory PerceptionFemalePsychologyPhotic StimulationDevelopmental Science
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Information structure in language acquisition. Production and comprehension of (in)definite articles by German-speaking children.

2020

AbstractThe present study investigates the production and comprehension of indefinite and definite articles as markers of givenness by typically-developing German-speaking children, from the perspective of information structure theory. The study involves 93 typically-developing children aged four to seven years old with normal language-skills and 20 adults. The results of a story-narration task and a truth-value judgment task reveal that children have more problems with new than with given referents in production as well as comprehension suggesting a “given better than new”-pattern. These findings are explained in the context of perspective-taking capacities and cue weighting theory.

AdultMaleLinguistics and LanguageExperimental and Cognitive PsychologyContext (language use)Language DevelopmentVocabulary050105 experimental psychologyLanguage and LinguisticsTask (project management)GermanGermanyDevelopmental and Educational PsychologyHumans0501 psychology and cognitive sciencesLanguage Development DisordersChildGeneral Psychology05 social sciencesPerspective (graphical)Information structurePragmaticsVerbal LearningLanguage acquisitionlanguage.human_languageComprehensionChild PreschoollanguageFemalePsychologyComprehensionChild Language050104 developmental & child psychologyCognitive psychologyJournal of child language
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Highly resilient coping entails better perceived health, high social support and low morning cortisol levels in parents of children with autism spect…

2013

The negative consequences of caring for people with developmental disabilities have been widely described. However, the ability to bounce back from the stress derived from care situations has been less studied. Those caregivers who have shown this ability are considered as resilient. This study aims to evaluate the relationship between resilience and self-reported health and cortisol awakening response (CAR) in a sample of caregivers of people with autism spectrum disorders (ASD). It also aims to evaluate the role of social support as a mediator in the association between resilience and health. Caregivers with higher resilience show better perceived health, lower morning cortisol levels, an…

AdultMaleParentsCoping (psychology)Cortisol awakening responseAdolescentHydrocortisoneHealth Statusmedia_common.quotation_subjectProtective factorLife Change EventsSocial supportSurveys and QuestionnairesAdaptation PsychologicalDevelopmental and Educational PsychologymedicineHumansChronic stressChildSalivamedia_commonSocial SupportMiddle AgedResilience Psychologicalmedicine.diseaseClinical PsychologyChild Development Disorders PervasiveAutism spectrum disorderAutismFemalePsychological resiliencePsychologyStress PsychologicalClinical psychologyResearch in Developmental Disabilities
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Early language and behavioral regulation skills as predictors of social outcomes.

2012

Purpose In the present study, the authors examined the prospective associations among early language skills, behavioral regulation skills, and 2 aspects of school-age social functioning (adaptability and social skills). Method The study sample consisted of children with and without a familial risk for dyslexia. The authors analyzed the relations among children’s language (at age 2;6 [years;months] and age 5;0), behavioral regulation skills (at age 5;0), and social functioning (at age 8;0) using structural equation modeling. Subgroups of children with respect to language and behavioral regulation skills (at age 5;0) were identified through the use of mixture modeling. Results Among at-risk …

AdultMaleParentsLinguistics and LanguageMediation (statistics)Adolescentmedia_common.quotation_subjecteducationChild BehaviorLife skillsModels PsychologicalLanguage DevelopmentLanguage and LinguisticsStructural equation modelingDevelopmental psychologyDyslexiaSpeech and HearingYoung AdultSocial skillsPredictive Value of TestsRisk FactorsAdaptation PsychologicalmedicineHumansLanguage Development DisordersLongitudinal StudiesSocial Behaviormedia_commonFamily HealthDyslexiaSelf-controlMiddle AgedLanguage acquisitionmedicine.diseaseLanguage developmentChild PreschoolFemalePsychologyChild LanguageJournal of speech, language, and hearing research : JSLHR
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A comparative study of sensory processing in children with and without Autism Spectrum Disorder in the home and classroom environments.

2015

Sensory processing and higher integrative functions impairments are highly prevalent in children with ASD. Context should be considered in analyzing the sensory profile and higher integrative functions. The main objective of this study is to compare sensory processing, social participation and praxis in a group of 79 children (65 males and 14 females) from 5 to 8 years of age (M=6.09) divided into two groups: ASD Group (n=41) and Comparison Group (n=38). The Sensory Processing Measure (SPM) was used to evaluate the sensory profile of the children: parents reported information about their children's characteristics in the home environment, and teachers reported information about the same cha…

AdultMaleParentsSensory processingmedicine.medical_treatmentContext (language use)Sensory profileEnvironmentSocial Environmentbehavioral disciplines and activitiesDevelopmental psychologyPerceptual DisordersStimulus modalitySurveys and Questionnairesmental disordersDevelopmental and Educational PsychologymedicineHumansChildSchoolsSocial environmentMiddle Agedmedicine.diseaseSocial engagementSocial ParticipationFacultyClinical PsychologyAutism spectrum disorderChild Development Disorders PervasiveCase-Control StudiesChild PreschoolFemalePerceptual DisordersPsychologyResearch in developmental disabilities
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Oral manifestations in a group of adults with autism spectrum disorder

2011

Objective: A number of studies have evaluated the oral health of patients with autism spectrum disorder (ASD), though most have involved children, and no specific oral manifestations have been described. The present study describes the buccodental disorders and hygiene habits in a group of adults with ASD. Study Design: A prospective case-control study was made of a group of patients with ASD (n=30), with a mean age of 27.7 +/- 5.69 years, and of a healthy age-and gender-matched control group (n=30). An evaluation was made of the medical history, medication, oral hygiene habits and oral diseases, with determination of the CAOD, CAOS and OHI-S oral hygiene scores. Results: Most of the patien…

AdultMalePediatricsmedicine.medical_specialtymedia_common.quotation_subjectPopulationDentistryOral hygieneYoung AdultHygienemental disordersmedicineHumansMedical historyProspective StudiesYoung adultAutism spectrum disorderChildProspective cohort studyeducationGeneral Dentistrymedia_commoncarieseducation.field_of_studybusiness.industryCase-control studyOdontostomatology for the Disabled or Special PatientOral Hygiene:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseoral manifestationsstomatognathic diseasesOtorhinolaryngologyChild Development Disorders PervasiveAutism spectrum disorderCase-Control StudiesUNESCO::CIENCIAS MÉDICASdental hygieneResearch-ArticleFemaleSurgeryMouth Diseasesbusiness
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Revisiting mu suppression in autism spectrum disorder

2014

Two aspects of the EEG literature lead us to revisit mu suppression in Autism Spectrum Disorder (ASD). First and despite the fact that the mu rhythm can be functionally segregated in two discrete sub-bands, 8-10 Hz and 10-12/13 Hz, mu-suppression in ASD has been analyzed as a homogeneous phenomenon covering the 8-13 Hz frequency. Second and although alpha-like activity is usually found across the entire scalp, ASD studies of action observation have focused on the central electrodes (C3/C4). The present study was aimed at testing on the whole brain the hypothesis of a functional dissociation of mu and alpha responses to the observation of human actions in ASD according to bandwidths. Electro…

AdultMale[ SDV.MHEP.PSM ] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental healthEntire scalpautism spectrum disorderElectroencephalographyaction observationYoung AdultRhythmmental disordersmedicineHumansEEGMolecular Biologymu-suppressiontop-down inhibitory controlCerebral Cortexmedicine.diagnostic_testGeneral NeuroscienceElectroencephalographyNeurophysiologymedicine.diseaseBrain WavesAlpha Rhythmmedicine.anatomical_structureChild Development Disorders PervasiveAutism spectrum disorderScalp[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental healthAction observationAutismFemaleNeurology (clinical)PsychologyNeuroscienceDevelopmental Biology
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Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort…

2015

Background The 17q21.31 deletion syndrome phenotype can be caused by either chromosome deletions or point mutations in the KANSL1 gene. To date, about 60 subjects with chromosome deletion and 4 subjects with point mutation in KANSL1 have been reported. Prevalence of chromosome deletions compared with point mutations, genotype–phenotype correlations and phenotypic variability have yet to be fully clarified. Methods We report genotype–phenotype correlations in 27 novel subjects with 17q21.31 deletion and in 5 subjects with KANSL1 point mutation , 3 of whom were not previously reported. Results The prevalence of chromosome deletion and KANSL1 mutation was 83% and 17%, respectively. All patient…

AdultMalemedicine.medical_specialtyAdolescentgenotype-phenotype correlationsKoolen De Vries syndromeKANSL1 mutationHaploinsufficiencyBiologySettore MED/03 - GENETICA MEDICASeverity of Illness IndexCraniofacial AbnormalitiesYoung AdultSeizuresMolecular geneticsGeneticsmedicineHumansAbnormalities MultipleLanguage Development DisordersChildGenetics (clinical)Genetic Association StudiesGeneticsOptic nerve hypoplasiaFetal Growth RetardationPoint mutationMacrocephalyInfantNuclear ProteinsSyndromeclinical heterogeneitySmith–Magenis syndromemedicine.diseaseChild PreschoolSpeech delayFemalemedicine.symptomChromosome DeletionSmith-Magenis SyndromeHaploinsufficiencyChromosomes Human Pair 1717q21.31 deletion
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