Search results for "Language Development Disorders"

showing 10 items of 32 documents

Understanding developmental language disorder-The Helsinki longitudinal SLI study (HelSLI): A study protocol

2018

Background Developmental language disorder (DLD, also called specific language impairment, SLI) is a common developmental disorder comprising the largest disability group in pre-school-aged children. Approximately 7% of the population is expected to have developmental language difficulties. However, the specific etiological factors leading to DLD are not yet known and even the typical linguistic features appear to vary by language. We present here a project that investigates DLD at multiple levels of analysis and aims to make the reliable prediction and early identification of the difficulties possible. Following the multiple deficit model of developmental disorders, we investigate the DLD …

MaleLongitudinal studyRJ101kielelliset häiriötSpecific language impairmentArtificial grammar learningpreschool child3124 Neurology and psychiatryDevelopmental psychologytemperamenttiStudy Protocol0302 clinical medicinekielellinen kehitysClinical ProtocolsChild temperamentkielen omaksuminenEEGLongitudinal Studies10. No inequalitykielen oppiminenGeneral PsychologyFinlandpathophysiologyeducation.field_of_studychild4. Education05 social sciencesNeuropsychologylongitudinal studyCognitionGeneral MedicineLanguage acquisitionLanguage acquisitionpsychology ChildP1femaleSpecific language impairmentChild Preschoolgeneettiset tekijätPsychologyEvent-related potentialsChild behaviormultilingualism515 Psychology(Nonverbal) short-term memoryPopulationlcsh:BF1-990developmental language disorderlapset (ikäryhmät)050105 experimental psychology03 medical and health sciencesDevelopmental language disorderoppimisvaikeudetmedicineGeneticsHumans0501 psychology and cognitive sciencesLanguage Development Disorders6121 Languageshumaneducationkielellinen erityisvaikeusperinnöllisyystiedeSequential bilingualismmedicine.diseasetyömuistiDevelopmental disorderlcsh:PsychologySequential bilingualismClinical EEGclinical protocol030217 neurology & neurosurgery
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Clinical significance of test refusal among young children.

2001

The present study describes the incidence of test refusal at neuropsychological assessment, investigates its correlates, and its stability. The participants were 124 children aged 3.5 years whose development has been followed from birth in the Jyvaskyla Longitudinal Study of Dyslexia (JLD). The frequency of test refusal on the Finnish version of the NEPSY was analyzed with respect to the children's concurrent and earlier cognitive and language skills, assessed using tests and parental ratings. Refusal during test-taking was found to be relatively common at this age, and high frequency of refusal at an earlier age was associated with similar tendency at a later age. High test refusal was ass…

MaleLongitudinal studyStatistics as TopicNeuropsychological TestsNEPSYDevelopmental psychologyDyslexiaDevelopmental and Educational PsychologymedicineHumansLanguage Development DisordersNeuropsychological assessmentLongitudinal StudiesDefense MechanismsRefusal to Participatemedicine.diagnostic_testIncidence (epidemiology)NeuropsychologyDyslexiaCognitionPatient Acceptance of Health Caremedicine.diseaseTest (assessment)Neuropsychology and Physiological PsychologyCross-Sectional StudiesChild PreschoolPediatrics Perinatology and Child HealthFemalePsychologyChild neuropsychology : a journal on normal and abnormal development in childhood and adolescence
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Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

2020

International audience; PURPOSE: Lamb-Shaffer syndrome (LAMSHF) is a neurodevelopmental disorder described in just over two dozen patients with heterozygous genetic alterations involving SOX5, a gene encoding a transcription factor regulating cell fate and differentiation in neurogenesis and other discrete developmental processes. The genetic alterations described so far are mainly microdeletions. The present study was aimed at increasing our understanding of LAMSHF, its clinical and genetic spectrum, and the pathophysiological mechanisms involved.METHODS: Clinical and genetic data were collected through GeneMatcher and clinical or genetic networks for 41 novel patients harboring various ty…

MaleMedizinHaploinsufficiencyL-SOX5VARIANTS0302 clinical medicineNeurodevelopmental disorderIntellectual disabilityMissense mutation2.1 Biological and endogenous factorsAetiologyChildGenetics (clinical)GeneticsPediatricGenetics & Heredity0303 health sciencesPedigreeFAMILYDNA-Binding Proteinsdevelopmental delayTRANSCRIPTION FACTORSPhenotypeintellectual disabilityChild Preschoolmissense variantsFemalemissense variants.HaploinsufficiencySOXD Transcription FactorsAdultEXPRESSIONAdolescentIntellectual and Developmental Disabilities (IDD)Clinical SciencesMutation MissenseautismCell fate determinationBiologyLONG FORMSEQUENCEArticle03 medical and health sciencesYoung AdultRare DiseasesClinical ResearchCARTILAGEIntellectual DisabilitymedicineGeneticsAnimalsHumansLanguage Development DisordersGenetic Predisposition to DiseasePreschoolTranscription factorGene030304 developmental biology[SDV.GEN]Life Sciences [q-bio]/GeneticsMUTATIONSHuman GenomeInfantmedicine.diseaseBrain DisordersNeurodevelopmental DisordersDeciphering Developmental Disorder StudyMutationAutismepilepsyMissense030217 neurology & neurosurgeryGENERATIONGenetics in Medicine
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Associations Between Toddler-Age Communication and Kindergarten-Age Self-Regulatory Skills

2014

Purpose In this study, the authors aimed at gaining understanding on the associations of different types of early language and communication profiles with later self-regulation skills by using longitudinal data from toddler age to kindergarten age. Method Children with early language profiles representing expressive delay, broad delay (i.e., expressive, social, and/or symbolic), and typical language development were compared in domains of kindergarten-age executive and regulative skills (attentional/executive functions, regulation of emotions and behavioral activity, and social skills) assessed with parental questionnaires. Results Children with delay in toddler-age language development de…

MaleParentsLinguistics and Languagemedia_common.quotation_subjecteducationitsesäätelyLanguage and LinguisticsSelf-ControlDevelopmental psychologySkills managementExecutive FunctionSpeech and HearingSocial skillsSurveys and QuestionnairesHumansAttentionLanguage Development DisordersLongitudinal StudiestoddlersToddlerChildSocial BehaviorEarly languageviestintämedia_commontaaperotskillscommunicationCommunicationtaidotInfantSelf-controlExecutive functionsLanguage acquisitionLanguage developmentself-regulatoryChild PreschoolRegression AnalysisFemalePsychologyChild LanguageJournal of Speech, Language, and Hearing Research
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Development of early motor skills and language in children at risk for familial dyslexia

2007

Differences in motor development and the relationship between motor and language development were studied in 88 children with familial risk for dyslexia (43 females, 45 males; at-risk group) and 88 children without familial risk for dyslexia (35 females, 53 females; control group; n=176) during the first two years of life. A structured parental questionnaire was used to assess motor development. Expressive language skills were assessed at the age of 18 months with the Reynell Developmental Language Scales and at 18 and 24 months with the MacArthur Communicative Development Inventories. At group level, the motor development of children in both the at-risk and control groups was similar. Howe…

MaleRiskVocabularyDevelopmental Disabilitiesmedia_common.quotation_subjectGross motor skillDevelopmental psychologyDyslexiaDevelopmental NeurosciencemedicineHumansGenetic Predisposition to DiseaseLanguage Development DisordersLongitudinal StudiesProspective StudiesChildGroup levelMotor skillmedia_commonNeurologic ExaminationLanguage TestsSignificant differenceInfant NewbornDyslexiaInfantExpressive languagemedicine.diseaseLanguage developmentMotor SkillsChild PreschoolPediatrics Perinatology and Child HealthFemaleNeurology (clinical)Psychomotor DisordersPsychologyDevelopmental Medicine & Child Neurology
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A pilot study of the effects of RightStart instruction on early numeracy skills of children with specific language impairment

2013

This pilot study investigated the effects of an early numeracy program, RightStart Mathematics (RS), on Finnish kindergartners with specific language impairment (SLI). The study applied a pre-test-instruction-post-test design. The children with SLI (n=9, Mage=82.11 months) received RS instruction two to three times a week for 40 min over seven months, which replaced their business-as-usual mathematics instruction. Mathematical skill development among children with SLI was examined at the individual and group levels, and compared to the performance of normal language-achieving age peers (n=32, Mage=74.16 months) who received business-as-usual kindergarten mathematics instruction. The childre…

MaleShort-term memoryPilot ProjectsSpecific language impairmentDevelopmental psychologyMathematical skillEarly Intervention EducationalDevelopmental and Educational PsychologymedicineHumansLanguage Development Disorders0501 psychology and cognitive sciencesChildMathematics instructionWorking memory4. Education05 social sciencesSignificant differenceSubtraction050301 educationmedicine.diseaseClinical PsychologyEarly numeracyFemalePsychology0503 educationMathematics050104 developmental & child psychologyResearch in Developmental Disabilities
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12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.

2012

Speech sound disorders are heterogeneous conditions, and sporadic and familial cases have been described. However, monogenic inheritance explains only a small proportion of such disorders, in particular in cases with childhood apraxia of speech (CAS). Deletions of <5 Mb involving the 12p13.33 locus is one of the least commonly deleted subtelomeric regions. Only four patients have been reported with such a deletion diagnosed with fluorescence in situ hybridisation telomere analysis or array CGH. To further delineate this rare microdeletional syndrome, a French collaboration together with a search in the Decipher database allowed us to gather nine new patients with a 12p13.33 subtelomeric or …

MaleSpeech productionApraxiasLocus (genetics)Nerve Tissue ProteinsBiologyArticlePregnancyGeneticsmedicineHumansSpeechFamilyGenetic Predisposition to DiseaseLanguage Development DisordersChildGeneGenetics (clinical)In Situ Hybridization FluorescenceAdaptor Proteins Signal TransducingGeneticsChromosomes Human Pair 12medicine.diseaseSubtelomereSpeech TherapistPhenotypeChild PreschoolChildhood apraxia of speechSpeech delayFemaleFrancemedicine.symptomChromosome DeletionEuropean journal of human genetics : EJHG
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Reading outcomes of children with delayed early vocabulary: A follow-up from age 2-16.

2018

Abstract Background Delays in expressive vocabulary have been associated with lower outcomes in reading. Aim The aim is to conduct a long-term follow-up study to investigate if early expressive vocabulary delay (late talking) predicts reading development in participants age 16 and under. We examine further if the prediction is different in the presence of family risk for dyslexia (FR) and early receptive vocabulary delay. Methods Expressive and receptive vocabulary skills were assessed at the age of 2–2.5 years, and reading skills in Grades 2, 3, 8 and 9 (age 8–16). The longitudinal sample consisted of 200 Finnish-speaking children, of which 108 had FR for dyslexia and 92 came from families…

MaleVocabularyAudiologyVocabularyDyslexiasanavarastoRisk FactorsReading (process)Developmental and Educational Psychologyta516reading difficultiesLongitudinal StudiesChildta515Finlandmedia_commonReceptive vocabularyluetun ymmärtäminenLanguage Tests05 social sciences050301 educationreading comprehensionPrognosisClinical PsychologyExpressive vocabularyChild PreschoolFemalePsychologyComprehension050104 developmental & child psychologyreceptive vocabularymedicine.medical_specialtyexpressive vocabularyAdolescentmedia_common.quotation_subjectFluencymedicineHumans0501 psychology and cognitive sciencesLanguage Development Disordersreading (activity)Late talkersDyslexialukeminen (toiminta)medicine.diseasereading fluencyReading comprehensionReadinglukutaitolukihäiriöt0503 educationFollow-Up StudiesResearch in developmental disabilities
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School-entry language outcomes in late talkers with and without a family risk of dyslexia.

2020

Children with familial risk (FR) of dyslexia and children with early language delay are known to be at risk for later language and literacy difficulties. However, research addressing long‐term outcomes in children with both risk factors is scarce. This study tracked FR and No‐FR children identified as late talkers at 2 years of age and reports development from 4;6 through 6 years. We examined the possible effects of FR‐status and late talking (LT) status, respectively, on language skills at school entry, and whether FR‐status moderated the associations between 4;6‐year and 6‐year language scores. Results indicated an effect of LT status on language at both ages, while FR status affected lan…

MaleVocabularyVocabularyLiteracypuheen kehitysDevelopmental psychologyDyslexiakielellinen kehityssanavarastoRisk FactorsDevelopmental and Educational PsychologyChildmedia_commonLanguage TestsGrammar05 social sciences050301 educationGeneral MedicinePeer reviewkielioppipuhe (puhuminen)Child PreschoolgrammarFemalePsychologyVDP::Social science: 200::Education: 280Child Languagemedia_common.quotation_subjectExperimental and Cognitive Psychology050105 experimental psychologyEducationmedicinedysleksiaHumans0501 psychology and cognitive sciencesGenetic Predisposition to DiseaseLanguage Development Disorderslate talkersAssociation (psychology)perinnöllisyysvocabularyDyslexiaLate talkersLinguisticsmedicine.diseaseVDP::Samfunnsvitenskap: 200::Pedagogiske fag: 280family risk of dyslexiaemerging developmental language disorderesikouluikäisetlukihäiriöt0503 educationOn LanguageDyslexia (Chichester, England)REFERENCES
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Developmental pathways of children with and without familial risk for dyslexia during the first years of life.

2002

Comparisons of the developmental pathways of the first 5 years of life for children with (N = 107) and without (N = 93) familial risk for dyslexia observed in the Jyvaskyla Longitudinal study of Dyslexia are reviewed. The earliest differences between groups were found at the ages of a few days and at 6 months in brain event-related potential responses to speech sounds and in head-turn responses (at 6 months), conditioned to reflect categorical perception of speech stimuli. The development of vocalization and motor behavior, based on parental report of the time of reaching significant milestones, or the growth of vocabulary (using the MacArthur Communicative Development Inventories) failed t…

Psychomotor learningRiskLongitudinal studyDevelopmental DisabilitiesGross motor skillDyslexiaInfant NewbornInfantmedicine.diseaseBayley Scales of Infant DevelopmentDevelopmental psychologyDyslexiaLanguage developmentNeuropsychology and Physiological PsychologyCommunication disorderChild PreschoolDevelopmental and Educational PsychologymedicineHumansLanguage disorderGenetic Predisposition to DiseaseLanguage Development DisordersLongitudinal StudiesPsychologyChildDevelopmental neuropsychology
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