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1.
Epilepsy Behav ; 59: 111-6, 2016 06.
Article de Anglais | MEDLINE | ID: mdl-27131051

RÉSUMÉ

The abnormal brain discharges observed in benign childhood epilepsy with centrotemporal spikes (BECTS) and temporal lobe epilepsy (TLE) are located close to areas responsible for auditory and language processing. This study aimed to analyze the results of auditory event-related potentials (P300) in children with BECTS and TLE in order to assess whether the epileptic activity in centrotemporal and temporal regions may compromise the integrity and physiology of auditory system structures. This was a prospective, comparative, and cross-sectional study. Group I (GI) consisted of 13 children diagnosed with BECTS, group II (GII), 7 children diagnosed with TLE, and control group (GIII), 16 healthy children, with no hearing or academic complaints. After neurological and basic audiological assessments, P300 was applied. The P300 latency and amplitude were compared between groups. Regarding latency, GI showed 324.1 (+31.5) ms, GII 336.3 (+23.5) ms, and GIII 318 (+27.7) ms. Amplitudes were 4.80 (+3.2) µV in GI, 4.7 (+2.5) µV in GII, and 5.8 (+2.4) µV in GIII. Although children with BECTS showed prolonged latencies and reduced amplitudes, these differences were not considered statistically significant. Children with TLE showed statistically significant prolonged P300 latency compared with the control group (P=0.037). We speculate that abnormal electrical discharges in centrotemporal and temporal regions led to the slowing of auditory processing in our sample.


Sujet(s)
Potentiels d'action/physiologie , Épilepsie rolandique/diagnostic , Épilepsie rolandique/physiopathologie , Épilepsie temporale/diagnostic , Épilepsie temporale/physiopathologie , Potentiels évoqués auditifs/physiologie , Stimulation acoustique/méthodes , Adolescent , Enfant , Enfant d'âge préscolaire , Études transversales , Femelle , Humains , Mâle , Études prospectives
2.
Epilepsy Behav ; 53: 180-3, 2015 Dec.
Article de Anglais | MEDLINE | ID: mdl-26580215

RÉSUMÉ

Because of the relationship between rolandic, temporoparietal, and centrotemporal areas and language and auditory processing, the aim of this study was to investigate language and central temporal auditory processing of children with epilepsy (rolandic epilepsy and temporal lobe epilepsy) and compare these with those of children without epilepsy. Thirty-five children aged between eight and 14 years old were studied. Two groups of children participated in this study: a group with childhood epilepsy (n=19), and a control group without epilepsy or linguistic changes (n=16). There was a significant difference between the two groups, with the worst performance in children with epilepsy for the gaps-in-noise test, right ear (p<0.001) and left ear (p<0.001) tests, and duration pattern test--naming (p=0.002) and humming (p=0.002). In auditory P300, there was no significant difference in latency (p=0.343) and amplitude (p=0.194) between the groups. There was a significant difference between the groups, with the worst performance in children with epilepsy, for the auditory-receptive vocabulary (PPVT) (p<0.001) and phonological working memory (nonwords repetition task) tasks (p=0.001). We conclude that the impairment of central temporal auditory processing and language skills may be comorbidities in children with rolandic epilepsy and temporal lobe epilepsy.


Sujet(s)
Troubles de la perception auditive/physiopathologie , Épilepsie rolandique/physiopathologie , Épilepsie temporale/physiopathologie , Troubles du langage/physiopathologie , Stimulation acoustique/méthodes , Adolescent , Perception auditive/physiologie , Troubles de la perception auditive/diagnostic , Troubles de la perception auditive/épidémiologie , Enfant , Études transversales , Épilepsie rolandique/diagnostic , Épilepsie rolandique/épidémiologie , Épilepsie temporale/diagnostic , Épilepsie temporale/épidémiologie , Potentiels évoqués cognitifs P300/physiologie , Femelle , Humains , Troubles du langage/diagnostic , Troubles du langage/épidémiologie , Mâle
3.
J Neurol ; 261(7): 1374-80, 2014 Jul.
Article de Anglais | MEDLINE | ID: mdl-24781839

RÉSUMÉ

Congenital bilateral perisylvian syndrome (CBPS) presents with heterogeneous clinical manifestations such as pseudobulbar palsy, language disorder, variable cognitive deficits, epilepsy, and perisylvian abnormalities (most frequently polymicrogyria) on imaging studies. We investigated the relationship between seizures and extent of gray matter (GM) and white matter (WM) abnormalities using voxel-based morphometry (VBM) of brain magnetic resonance imaging (MRI) as well the association between seizures, structural abnormalities and cognitive ability. In this cross-sectional study, we evaluated 51 healthy volunteers and 18 patients with CBPS with epilepsy (seizure group, n = 7) and without (non-seizure group, n = 11). We used VBM (SPM8/DARTEL) to investigate areas with excess and atrophy of both gray and white matter, comparing groups of patients with controls. Intellectual ability of patients was assessed by the WISC-III or WAIS-III. Both groups with CBPS and the control group were homogeneous with respect to gender (p = 0.07) and age (p = 0.065). Besides perisylvian polymicrogyria, the seizure group exhibited areas with GM and WM reduction including temporal, frontal, parietal and occipital lobes. In contrast, we identified fewer areas with GM and WM reduction in the non-seizure group. The seizure group presented worse intellectual performance (performance IQ and global IQ) than the non-seizure group. The seizure group presented with a more widespread pattern of cortical and sub-cortical abnormalities, as well as worse cognition. Our results suggest that patients with CBPS and epilepsy appear to have widespread neuronal damage that goes beyond the areas with MRI-visible perisylvian polymicrogyria.


Sujet(s)
Malformations multiples/anatomopathologie , Encéphale/anatomopathologie , Troubles de la cognition/étiologie , Déficience intellectuelle/complications , Déficience intellectuelle/anatomopathologie , Intelligence/physiologie , Malformations corticales/complications , Malformations corticales/anatomopathologie , Adolescent , Adulte , Enfant , Enfant d'âge préscolaire , Études transversales , Électroencéphalographie , Épilepsie/étiologie , Épilepsie/anatomopathologie , Femelle , Humains , Traitement d'image par ordinateur , Imagerie par résonance magnétique , Mâle , Tests neuropsychologiques , Études rétrospectives , Statistique non paramétrique , Tomodensitométrie , Jeune adulte
4.
Epilepsy Behav ; 24(4): 403-7, 2012 Aug.
Article de Anglais | MEDLINE | ID: mdl-22683244

RÉSUMÉ

Rolandic epilepsy (RE) is the most common type of childhood focal epilepsy. Although there is no intellectual deficit, children with RE may have specific cognitive impairments. The aims of this study were to identify changes in executive functions in children with RE and to verify the influence of epilepsy and seizure variables. We evaluated 25 children with RE and 28 healthy controls. A comprehensive neuropsychological battery was utilized. The results showed that the RE children had worse performance than the control group in some categories of the Wisconsin Card Sorting Test, the Trail Making Test part B, and the Verbal Fluency Test (FAS). Children with earlier onset of epilepsy had worse performance when compared with children with later onset of epilepsy. We conclude that children with RE may show a deficit in executive function despite their normal IQ. The set of tests was more extensive than what was previously used in other studies. Our study suggests that early seizures can interfere with brain development. Regarding cognition, the term benign should be used cautiously in RE.


Sujet(s)
Troubles de la cognition/diagnostic , Troubles de la cognition/étiologie , Épilepsie rolandique/complications , Fonction exécutive/physiologie , Tests neuropsychologiques , Enfant , Épilepsie rolandique/psychologie , Femelle , Humains , Mâle , Indice de gravité de la maladie , Statistiques comme sujet
5.
Brain Dev ; 33(10): 824-31, 2011 Nov.
Article de Anglais | MEDLINE | ID: mdl-21216548

RÉSUMÉ

Malformations of cortical development have been described in children and families with language-learning impairment. The objective of this study was to assess the auditory processing information in children with language-learning impairment in the presence or absence of a malformation of cortical development in the auditory processing areas. We selected 32 children (19 males), aged eight to 15 years, divided into three groups: Group I comprised 11 children with language-learning impairment and bilateral perisylvian polymicrogyria, Group II comprised 10 children with language-learning impairment and normal MRI, and Group III comprised 11 normal children. Behavioral auditory tests, such as the Random Gap Detection Test and Digits Dichotic Test were performed. Statistical analysis was performed using the Kruskal-Wallis test and Mann-Whitney test, with a level of significance of 0.05. The results revealed a statistically significant difference among the groups. Our data showed abnormalities in auditory processing of children in Groups I and II when compared with the control group, with children in Group I being more affected than children in Group II. Our data showed that the presence of a cortical malformation correlates with a worse performance in some tasks of auditory processing function.


Sujet(s)
Cortex auditif/anatomopathologie , Troubles de la perception auditive/complications , Troubles de la perception auditive/anatomopathologie , Troubles du développement du langage/complications , Troubles du développement du langage/anatomopathologie , Adolescent , Enfant , Femelle , Tests auditifs , Humains , Tests d'intelligence , Tests du langage , Imagerie par résonance magnétique , Mâle , Examen neurologique , Tests neuropsychologiques , Études rétrospectives , Statistique non paramétrique
6.
Pró-fono ; 22(4): 537-542, out.-dez. 2010. ilus, tab
Article de Portugais | LILACS | ID: lil-572526

RÉSUMÉ

TEMA: processamento temporal auditivo e dislexia do desenvolvimento. OBJETIVO: caracterizar o processamento temporal auditivo em escolares com dislexia do desenvolvimento e correlacionar com malformação cortical. MÉTODO: foram avaliados 20 escolares, com idade entre 8 e 14 anos, divididos em grupo experimental (GE) composto por 11 escolares (oito do gênero masculino) com o diagnóstico de dislexia do desenvolvimento e grupo controle (GC) composto por nove escolares (seis do gênero masculino) sem alterações neuropsicolinguísticas. Após avaliações neurológica, neuropsicológica e fonoaudiológica (avaliação de linguagem e leitura e escrita) para obtenção do diagnóstico, os escolares foram submetidos à avaliação audiológica periférica e posteriormente aplicou-se o teste Random Gap Detection Test e/ou Random Gap Detection Test Expanded. RESULTADOS: observou-se diferença estatisticamente significante entre os escolares do GE e GC, com pior desempenho para o GE. A maioria dos escolares do GE apresentou polimicrogiria perisylviana. CONCLUSÃO: escolares com dislexia do desenvolvimento podem apresentar alterações no processamento temporal auditivo com prejuízo no processamento fonológico. Malformação do desenvolvimento cortical pode ser o substrato anatômico dos distúrbios.


BACKGROUND: temporal auditory processing and developmental dyslexia. AIM: to characterize the temporal auditory processing in children with developmental dyslexia and to correlate findings with cortical malformations. METHOD: twenty school-aged children, ranging in age from 8 to 14 years were evaluated. These children were divided into two groups: the experimental group (EG) was composed by 11 children (eight were male) with developmental dyslexia and the control group (CG) was composed by nine normal children (six were male). After neurological assessment and verification of the intellectual level, language, reading and writing skills in order to determine the diagnosis, children underwent a peripheral audiological evaluation and Random Gap Detection Test and/or Random Gap Detection Test Expanded. RESULTS: a statistically significant difference between children in the EG and CG were observed, with children in the EG presenting worst performances. Most of the children in the EG presented perisylvian polymicrogyria. CONCLUSION: children with developmental dyslexia may present temporal auditory processing disorders with deficits in phonological processing. Cortical malformations may be the anatomical substrate of these disorders.


Sujet(s)
Adolescent , Enfant , Femelle , Humains , Mâle , Cortex auditif/physiopathologie , Perception auditive/physiologie , Dyslexie/physiopathologie , Malformations corticales/physiopathologie , Malformations multiples/physiopathologie , Études cas-témoins , Dyslexie/complications , Tests auditifs , Tests d'intelligence , Troubles du langage/étiologie , Déficience intellectuelle/physiopathologie , Tests neuropsychologiques , Répartition par sexe , Facteurs temps
7.
Pro Fono ; 22(4): 537-42, 2010.
Article de Anglais, Portugais | MEDLINE | ID: mdl-21271113

RÉSUMÉ

BACKGROUND: Temporal auditory processing and developmental dyslexia. AIM: To characterize the temporal auditory processing in children with developmental dyslexia and to correlate findings with cortical malformations. METHOD: Twenty school-aged children, ranging in age from 8 to 14 years were evaluated. These children were divided into two groups: the experimental group (EG) was composed by 11 children (eight were male) with developmental dyslexia and the control group (CG) was composed by nine normal children (six were male). After neurological assessment and verification of the intellectual level, language, reading and writing skills in order to determine the diagnosis, children underwent a peripheral audiological evaluation and Random Gap Detection Test and/or Random Gap Detection Test Expanded. RESULTS: A statistically significant difference between children in the EG and CG were observed, with children in the EG presenting worst performances. Most of the children in the EG presented perisylvian polymicrogyria. CONCLUSION: Children with developmental dyslexia may present temporal auditory processing disorders with deficits in phonological processing. Cortical malformations may be the anatomical substrate of these disorders.


Sujet(s)
Cortex auditif/physiopathologie , Perception auditive/physiologie , Dyslexie/physiopathologie , Malformations corticales/physiopathologie , Malformations multiples/physiopathologie , Adolescent , Études cas-témoins , Enfant , Dyslexie/complications , Femelle , Tests auditifs , Humains , Déficience intellectuelle/physiopathologie , Tests d'intelligence , Troubles du langage/étiologie , Mâle , Tests neuropsychologiques , Répartition par sexe , Facteurs temps
8.
Brain Dev ; 32(4): 299-304, 2010 Apr.
Article de Anglais | MEDLINE | ID: mdl-19410403

RÉSUMÉ

We hypothesized that the processing of auditory information by the perisylvian polymicrogyric cortex may be different from the normal cortex. To characterize the auditory processing in bilateral perisylvian syndrome, we examined ten patients with perisylvian polymicrogyria (Group I) and seven control children (Group II). Group I was composed by four children with bilateral perisylvian polymicrogyria and six children with bilateral posterior perisylvian polymicrogyria. The evaluation included neurological and neuroimaging investigation, intellectual quotient and audiological assessment (audiometry and behavior auditory tests). The results revealed a statistically significant difference between the groups in the behavioral auditory tests, such as, digits dichotic test, nonverbal dichotic test (specifically in right attention), and random gap detection/random gap detection expanded tests. Our data showed abnormalities in the auditory processing of children with perisylvian polymicrogyria, suggesting that perisylvian polymicrogyric cortex is functionally abnormal. We also found a correlation between the severity of our auditory findings and the extent of the cortical abnormality.


Sujet(s)
Troubles de la perception auditive/physiopathologie , Cortex cérébral/malformations , Malformations corticales , Adolescent , Audiométrie , Perception auditive/physiologie , Enfant , Femelle , Humains , Mâle , Malformations corticales/anatomopathologie , Malformations corticales/physiopathologie , Tests neuropsychologiques , Syndrome
9.
Braz J Otorhinolaryngol ; 75(2): 213-20, 2009.
Article de Anglais | MEDLINE | ID: mdl-19575106

RÉSUMÉ

UNLABELLED: Many children with auditory processing disorders have a high prevalence of otitis media, a middle ear alterations greatly prevalent in children with palatine and lip clefts. AIM: To check the performance of children with palate cleft alone (PC) in auditory processing tests. Prospective study. MATERIALS AND METHODS: Twenty children (7 to 11 years) with CP were submitted to sound location tests (SL), memory for verbal sounds (MSSV) and non verbal sounds in sequence (MSSNV), Revised auditory fusion (AFT-R), Pediatric test of speech intelligibility/synthetic sentences (PSI/SSI), alternate disyllables (SSW) and digit dichotic (DD). The children performances in the tests were classified in bad and good. RESULTS: There was no statistically significant difference between genders and ears. The average values obtained were 2.16, 2.42, 4.37, 60.50 ms; 40.71 to 67.33%; 96.25 to 99.38%; 73.55 to 73.88% and 58.38 to 65.47% respectively for the MSSNV, MSSV, LS, AFT-R, PSI/SSI tests with ipsilateral (PSI/SSIMCI) and contralateral (PSI/SSI/MCC) competitive message, DD and SSW tests. CONCLUSION: A high percentage of children showed worse results in the AFT-R, DD, SSW tests and in the PSI/SSIMCI tests. The best performances happened in the sound location tests, verbal and non-verbal sounds for sequential memory and for PSI/SSIMCC tests.


Sujet(s)
Audiométrie tonale , Perception auditive/physiologie , Troubles de la perception auditive/physiopathologie , Fente palatine/physiopathologie , Troubles de l'audition/physiopathologie , Troubles de la perception auditive/diagnostic , Troubles de la perception auditive/étiologie , Seuil auditif/physiologie , Enfant , Femelle , Troubles de l'audition/diagnostic , Humains , Mâle , Mémoire/physiologie , Son (physique) , Intelligibilité de la parole/physiologie , Perception de la parole/physiologie
12.
Rev. bras. otorrinolaringol ; 75(2): 213-220, mar.-abr. 2009. tab
Article de Portugais, Anglais | LILACS | ID: lil-517159

RÉSUMÉ

Muitas crianças com transtorno de processamento auditivo têm uma prevalência alta de otite média, alteração na orelha média de grande ocorrência na população com fissura labiopalatina. OBJETIVO: Verificar o desempenho de crianças com fissura isolada de palato (FP) em testes do processamento auditivo. Estudo prospectivo. MATERIAL E MÉTODO: Vinte crianças (7 a 11 anos) com FP foram submetidas aos testes de localização sonora (LS), memória para sons verbais (MSSV) e não-verbais em seqüência (MSSNV), Fusão Auditiva-Revisado (AFT-R), Teste Pediátrico de Inteligibilidade de Fala/Sentenças Sintéticas (PSI/SSI), Dissílabos alternados (SSW) e Dicótico de dígitos (DD). O desempenho das crianças nos testes foi classificado em ruim e bom. RESULTADOS: Não houve diferença estatística entre os gêneros e orelhas. Os valores médios obtidos foram 2,16, 2,42, 4,37, 60,50ms, de 40,71 a 67,33 por cento, 96,25 a 99,38 por cento, 73,55 a 73,88 por cento e 58,38 a 65,47 por cento, respectivamente, para os testes MSSNV, MSSV, LS, AFT-R, PSI/SSI com mensagem competitiva ipsilateral (PSI/SSIMCI) e contralateral (PSI/SSI/MCC), DD e SSW. CONCLUSÃO: Uma alta porcentagem de crianças demonstrou seus piores desempenhos nos testes AFT-R, DD, SSW e no teste PSI/SSIMCI. Os melhores desempenhos ocorreram nos testes de localização sonora, memória seqüencial para sons não verbais e verbais e para PSI/SSIMCC.


Many children with auditory processing disorders have a high prevalence of otitis media, a middle ear alterations greatly prevalent in children with palatine and lip clefts. AIM: to check the performance of children with palate cleft alone (PC) in auditory processing tests. Prospective study. MATERIALS AND METHODS: twenty children (7 to 11 years) with CP were submitted to sound location tests (SL), memory for verbal sounds (MSSV) and non verbal sounds in sequence (MSSNV), Revised auditory fusion (AFT-R), Pediatric test of speech intelligibility/synthetic sentences (PSI/SSI), alternate disyllables (SSW) and digit dichotic (DD). The children performances in the tests were classified in bad and good. RESULTS: there was no statistically significant difference between genders and ears. The average values obtained were 2.16, 2.42, 4.37, 60.50ms; 40.71 to 67.33 percent; 96.25 to 99.38 percent; 73.55 to 73.88 percent and 58.38 to 65.47 percent respectively for the MSSNV, MSSV, LS, AFT-R, PSI/SSI tests with ipsilateral (PSI/SSIMCI) and contralateral (PSI/SSI/MCC) competitive message, DD and SSW tests. CONCLUSION: a high percentage of children showed worse results in the AFT-R, DD, SSW tests and in the PSI/SSIMCI tests. The best performances happened in the sound location tests, verbal and non-verbal sounds for sequential memory and for PSI/SSIMCC tests.


Sujet(s)
Enfant , Femelle , Humains , Mâle , Audiométrie tonale , Perception auditive/physiologie , Troubles de la perception auditive/physiopathologie , Fente palatine/physiopathologie , Troubles de l'audition/physiopathologie , Troubles de la perception auditive/diagnostic , Troubles de la perception auditive/étiologie , Seuil auditif/physiologie , Troubles de l'audition/diagnostic , Mémoire/physiologie , Son (physique) , Intelligibilité de la parole/physiologie , Perception de la parole/physiologie
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