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1.
Child Care Health Dev ; 50(2): e13239, 2024 03.
Artigo em Inglês | MEDLINE | ID: mdl-38413377

RESUMO

BACKGROUND: Preterm children are at increased risk of cognitive and language delay compared with term-born children. While many perinatal factors associated with prematurity are well established, there is limited research concerning the influence of the socio-familial environment on the development of preterm children. This study aims to assess the relative impact of perinatal and socio-familial risk factors on cognitive and language development at 2 years corrected age (CA). METHOD: This retrospective cross-sectional study included preterm infants with a gestational age <32 weeks and/or a birth weight <1500 g, who underwent neurodevelopmental assessment at 2 years CA. Cognitive and language scores were assessed using the Bayley Scales of Infant-Toddler Development, third edition. Adjusted odds ratios (aORs) with 95% confidence intervals (CIs) were calculated using a multivariable model to examine the relationship between developmental delays and perinatal and socio-familial factors. RESULT: The prevalence of language delay was negatively associated with daycare attendance (aOR: 0.25, 95% CI: 0.07-0.85, p < 0.05) and high maternal educational levels (aOR: 0.24, 95% CI: 0.05-0.93, p < 0.05) and positively associated with bilingual environments (aOR: 5.62, 95% CI: 1.46-24.3, p < 0.05). Perinatal and postnatal risk factors did not show a significant impact on cognitive or language development. CONCLUSION: The development of language appears to be more influenced by the socio-familial environment than by early perinatal and postnatal factors associated with prematurity. These findings highlight the importance of considering socio-familial factors in the early identification and intervention of language delay among preterm children.


Assuntos
Lactente Extremamente Prematuro , Transtornos do Desenvolvimento da Linguagem , Lactente , Gravidez , Feminino , Criança , Recém-Nascido , Humanos , Lactente Extremamente Prematuro/psicologia , Deficiências do Desenvolvimento/epidemiologia , Estudos Retrospectivos , Estudos Transversais , Desenvolvimento da Linguagem , Desenvolvimento Infantil , Idade Gestacional , Transtornos do Desenvolvimento da Linguagem/etiologia , Transtornos do Desenvolvimento da Linguagem/complicações , Cognição , Recém-Nascido de muito Baixo Peso
2.
Neuropsychologia ; 196: 108817, 2024 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-38355036

RESUMO

Extent evidence has shown that morphosyntax is one of the most challenging linguistic areas for children with atypical early language experiences. Over the last couple of years, comparisons between deaf children with CIs and children with DLD have gained interest - as cases of atypical early language experiences, including, but not restricted to, delayed onset of exposure to language input and language-processing difficulties. Evidence suggests that the morphosyntactic difficulties experienced by deaf children with CIs and children with DLD are very similar in nature. However, the few studies that have directly compared both groups are inconclusive, with deaf children with CIs either performing significantly better or on par with children with DLD. These differences in findings can be attributed, in part at least, to a failure to implement essential methodological controls - even more so given that deaf children with CIs comprise a very diverse population. The goal of the present study was to directly compare the performance of deaf children with CIs to that of children with DLD on a morphosyntactic ability known to be particularly difficult for both groups. Specifically, the present study conducted a detailed examination of the past tense marking abilities of deaf children with CIs and children with DLD while controlling for factors specific to deaf children with CIs, for children's basic cognitive abilities as well as for children's age, sex assigned at birth, and SES. Past tense verbs are particularly relevant as they are used as a marker of developmental language disorder (DLD) in children learning French. Moreover, extent evidence shows that deaf children with CIs and children with DLD have important WM difficulties, but also that there is an association between auditory perception, processing abilities, and working memory (WM) abilities as well as with the acquisition of morphological features, including tense marking. Unfortunately, no study has examined the relation between the accurate production of past tense verbs and WM abilities in children with CIs and children with DLD learning French. Fifteen deaf children with CIs between 5 and 7 years of age were compared to 15 children with DLD and to 15 typically-developing monolingual controls (MON), matched on important variables, using a past tense elicitation task as well as measures of phonological and nonverbal WM abilities. The results confirm that the deaf children with CIs and the children with DLD both performed significantly lower than the MON controls on the past tense elicitation task - suggesting that difficulties with past tense verbs in French might not only be a marker of DLD but, instead, a correlate of atypical language acquisition. Of importance, the present study is the first to show that deaf children with CIs perform significantly lower than children with DLD on a past tense elicitation task - highlighting the importance of using methodological controls. As well, significant correlations were found between the performance of the deaf children with CIs and of the children with DLD on the past tense elicitation task and their phonological and nonverbal WM abilities. Taken together with previous studies conducted in the same populations, this represents another evidence suggesting that early atypical language experiences result in language and WM deficits, including morphosyntactic difficulties.


Assuntos
Implantes Cocleares , Transtornos do Desenvolvimento da Linguagem , Criança , Recém-Nascido , Humanos , Memória de Curto Prazo , Transtornos do Desenvolvimento da Linguagem/etiologia , Idioma , Transtornos da Memória , Testes de Linguagem
3.
Br J Oral Maxillofac Surg ; 62(1): 30-37, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-38057178

RESUMO

This review provides a comprehensive overview of the literature on velopharyngeal insufficiency, associated anomalies, and speech/language impairment in patients with craniofacial microsomia (CFM). A systematic search of the literature was conducted to identify records on VPI and speech impairment in CFM from their inception until September 2022 within the databases Embase, PubMed, MEDLINE, Ovid, CINAHL EBSCO, Web of Science, Cochrane, and Google Scholar. Seventeen articles were included, analysing 1,253 patients. Velopharyngeal insufficiency results in hypernasality can lead to speech impairment. The reported prevalence of both velopharyngeal insufficiency and hypernasality ranged between 12.5% and 55%, while the reported prevalence of speech impairment in patients with CFM varied between 35.4% and 74%. Language problems were reported in 37% to 50% of patients. Speech therapy was documented in 45.5% to 59.6% of patients, while surgical treatment for velopharyngeal insufficiency consisted of pharyngeal flap surgery or pharyngoplasty and was reported in 31.6% to 100%. Cleft lip and/or palate was reported in 10% to 100% of patients with CFM; these patients were found to have worse speech results than those without cleft lip and/or palate. No consensus was found on patient characteristics associated with an increased risk of velopharyngeal insufficiency and speech/language impairment. Although velopharyngeal insufficiency is a less commonly reported characteristic of CFM than other malformations, it can cause speech impairment, which may contribute to delayed language development in patients with CFM. Therefore, timely recognition and treatment of speech impairment is essential.


Assuntos
Fenda Labial , Fissura Palatina , Síndrome de Goldenhar , Transtornos do Desenvolvimento da Linguagem , Insuficiência Velofaríngea , Humanos , Insuficiência Velofaríngea/epidemiologia , Fala , Fenda Labial/cirurgia , Fissura Palatina/complicações , Fissura Palatina/cirurgia , Resultado do Tratamento , Distúrbios da Fala/epidemiologia , Distúrbios da Fala/etiologia , Distúrbios da Fala/cirurgia , Transtornos do Desenvolvimento da Linguagem/epidemiologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Estudos Retrospectivos
4.
Child Abuse Negl ; 146: 106448, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37722293

RESUMO

BACKGROUND: Neglected children are at high risk for significant difficulties in speech and language development. Because no longitudinal study has been conducted to date, the dynamic description of development during the preschool period is unknown. OBJECTIVES: Establish the developmental trajectories of speech sounds, receptive and expressive vocabulary, and morphosyntax among neglected children during the preschool years and compare them with those of non-neglected children. PARTICIPANTS AND SETTING: Participants are 69 neglected children and 99 same age non-neglected peers (37 and 46 males respectively) recruited at 36 months of age. Data were collected at home. METHODS: Data were collected at six-month intervals between the ages of 3 and 5.5 years using psychometrically robust tools. Neglected and control groups were compared according to age using repeated measures ANOVAs on all variables. A discrete mixture model for clustering longitudinal data was used for testing the heterogeneity of the language trajectories among neglected children. RESULTS: The language development of the neglected children as a whole group is lower than that of the control group for all variables. Two subgroups are identified within the neglected group: one with a developmental trajectory similar to that of the non-neglected children, and another whose trajectory is far below that of the control group. The effect sizes of these differences vary between 1.4 and 3 standard deviations under the mean. CONCLUSIONS: A large proportion of neglected children present significant speech and language difficulties from the age of 3, but some of them catch up and develop similarly to non-neglected children.


Assuntos
Transtornos do Desenvolvimento da Linguagem , Fala , Masculino , Humanos , Pré-Escolar , Criança , Transtornos do Desenvolvimento da Linguagem/epidemiologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Idioma , Desenvolvimento da Linguagem , Estudos Longitudinais
5.
Neurosci Biobehav Rev ; 154: 105398, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37741516

RESUMO

Language is a complex multidimensional cognitive system that is connected to many neurocognitive capacities. The development of language is therefore strongly intertwined with the development of these capacities and their neurobiological substrates. Consequently, language problems, for example those of children with Developmental Language Disorder (DLD), are explained by a variety of etiological pathways and each of these pathways will be associated with specific risk factors. In this review, we attempt to link previously described factors that may interfere with language development to putative underlying neurobiological mechanisms of language development, hoping to uncover openings for future therapeutical approaches or interventions that can help children to optimally develop their language skills.


Assuntos
Transtornos do Desenvolvimento da Linguagem , Criança , Humanos , Transtornos do Desenvolvimento da Linguagem/etiologia , Transtornos do Desenvolvimento da Linguagem/psicologia , Desenvolvimento da Linguagem , Fatores de Risco
7.
J Speech Lang Hear Res ; 66(1): 190-205, 2023 01 12.
Artigo em Inglês | MEDLINE | ID: mdl-36525624

RESUMO

PURPOSE: Caregivers of autistic children present with high stress levels, which have been associated with poorer child outcomes in several domains, including language development. However, prior to this study, it was unknown whether elevated caregiver stress was associated with language development in infant siblings of autistic children (Sibs-autism), who are at increased likelihood of receiving a future diagnosis of autism and/or language impairment compared to infant siblings of non-autistic children. This study explored the degree to which, as well as the mechanisms by which, caregiver stress was linked with later language outcomes of Sibs-autism and infant siblings of non-autistic children (Sibs-NA). METHOD: Participants were 50 infants (28 Sibs-autism; 22 Sibs-NA) aged 12-18 months at the first time point in this study (Time 1). Infants were seen again 9 months later, at 21-27 months of age (Time 2). Caregiver stress was measured via a validated self-report measure at Time 1. Caregiver language input, the putative mechanism by which caregiver stress may influence later language outcomes, was collected via two daylong recordings from digital recording (Language ENvironment Analysis) devices worn by the child at this same time point. Child language outcomes were measured via standardized and caregiver report measures at Time 2. RESULTS: Several models testing hypothesized indirect effects of caregiver stress on later child language outcomes through caregiver language input were statistically significant. Specifically, significant indirect effects suggest that (a) caregivers with increased stress tend to speak less to their infants, and (b) this reduced language input tends to covary with reduced child language outcomes later in life for Sibs-autism and Sibs-NA. CONCLUSIONS: This study provides new insights into links between caregiver stress, caregiver language input, and language outcomes in Sibs-autism and Sibs-NA. Further work is necessary to understand how to best support caregivers and optimize the language learning environments for infants. SUPPLEMENTAL MATERIAL: https://doi.org/10.23641/asha.21714368.


Assuntos
Transtorno Autístico , Transtornos do Desenvolvimento da Linguagem , Criança , Humanos , Lactente , Irmãos , Desenvolvimento Infantil , Cuidadores , Transtornos do Desenvolvimento da Linguagem/etiologia , Transtornos do Desenvolvimento da Linguagem/diagnóstico
8.
Rev. otorrinolaringol. cir. cabeza cuello ; 82(3): 383-390, sept. 2022. ilus, tab
Artigo em Espanhol | LILACS | ID: biblio-1409950

RESUMO

Resumen La otitis media constituye una de las consultas médicas más comunes en la población infantil. Se caracteriza por la inflamación del oído medio en presencia de exudado en la cavidad timpánica, abarcando un amplio espectro de formas clínicas, dentro de las que destacan la otitis media aguda, con efusión y crónica. La hipoacusia de conducción es una de las complicaciones de la otitis media, por lo que es lógico pensar que algunas habilidades del lenguaje y cognición infantil podrían verse afectadas secundariamente. Sin embargo, la evidencia en torno al tema no es concluyente y se aprecian opiniones contrapuestas; asimismo, no existe actualmente una revisión de la literatura que agrupe las investigaciones existentes en torno al tema. Por ello, el presente estudio pretende identificar y analizar la evidencia científica disponible sobre el efecto de la otitis media en el desarrollo de la cognición y lenguaje infantil. Se realizó una revisión de la literatura guiada por protocolo PRISMA en bases de datos de acuerdo a términos claves. Fueron analizados 8 artículos que cumplieron con los criterios de inclusión. Los resultados recabados sugieren, por una parte, que la otitis media afecta el lenguaje en sus distintas dimensiones, el vocabulario comprensivo y la longitud media del enunciado; mientras que, por otra parte, no se encontró efecto directo de la otitis media o hipoacusia sobre la comprensión del lenguaje. Se concluye que las investigaciones analizadas presentan gran variabilidad de resultados y conclusiones. No existen reportes sobre su impacto en otros dominios de la cognición.


Abstract Otitis media is one of the most common medical consultations in children. It is characterized by inflammation of the middle ear in the presence of exudate in the tympanic cavity, covering a wide spectrum of clinical forms, among which acute otitis media, otitis media with effusion and chronic otitis media are the most outstanding. Conductive hearing loss is one of the complications of otitis media, so it is logical to think that some language and cognitive skills in children could be affected. However, the evidence on this matter is not conclusive and there are conflicting opinions; likewise, there is currently no review of the literature that compile the existing research on this topic. Therefore, the present study aims to identify and analyze the available scientific evidence on the effect of otitis media on the development of children's cognition and language. A review of the literature, guided by PRISMA protocol, was conducted in databases according to key terms. Eight articles that met the inclusion criteria were analyzed. The results suggest, on the one hand, that otitis media affects language in its different dimensions, comprehensive vocabulary and average sentence length; while on the other hand, no direct effect of otitis media or hearing loss on language comprehension was found. In is concluded that the research that were analyzed present great variability of results and conclusions. There are no reports on its impact on other domains of cognition.


Assuntos
Humanos , Criança , Otite Média/complicações , Cognição/fisiologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Qualidade de Vida , Linguagem Infantil , Perda Auditiva Condutiva/etiologia
9.
J Paediatr Child Health ; 58(11): 2044-2050, 2022 11.
Artigo em Inglês | MEDLINE | ID: mdl-35922883

RESUMO

AIM: This study sought to determine the prevalence of Developmental Language Disorder (DLD) in Australian school-aged children and associated potential risk factors for DLD at 10 years. METHODS: This study used a cross-sectional design to estimate the prevalence of DLD in Generation 2 of the prospective Raine Study. Participants included 1626 children aged 10 years with available language data. Primary outcomes included variables matching diagnostic criteria for DLD. Associations of other potential prenatal and environmental variables were analysed as secondary outcomes. RESULTS: The prevalence of DLD in this sample was 6.4% (n = 104) at 10 years. This sub-cohort comprised 33.7% (n = 35) with expressive language deficits, 20.2% (n = 21) with receptive language deficits, and 46.2% (n = 48) with receptive-expressive deficits. No significant difference in sex distribution was observed (52.9% male, p = 0.799). Children who were exposed to smoke in utero at 18 weeks gestation were at increased risk of DLD at 10 years (OR = 2.56, CI = 1.23-5.35, p = 0.012). CONCLUSIONS: DLD is a relatively prevalent condition in Australian children, even when assessed in middle childhood years. These findings can inform future research priorities, and public health and educational policy which account for the associations with potential risk factors.


Assuntos
Transtornos do Desenvolvimento da Linguagem , Criança , Humanos , Masculino , Feminino , Transtornos do Desenvolvimento da Linguagem/epidemiologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Prevalência , Estudos Prospectivos , Estudos Transversais , Austrália/epidemiologia , Fatores de Risco
10.
J Neurodev Disord ; 14(1): 38, 2022 06 17.
Artigo em Inglês | MEDLINE | ID: mdl-35715727

RESUMO

BACKGROUND: Late talking (LT) in toddlers is a risk factor for language weakness that may interfere with the development of using language to regulate behavior and emotion and contribute to the development of behavior problems from early childhood. This study examined the temporal stability of parent-reported behavior problems among Mandarin-speaking LT toddlers from ages 2 to 4 in Taiwan. METHODS: Thirty-one LT and 31 typical language development (TLD) toddlers were assessed for their vocabulary production at age 2 with the Words and Sentences Forms of the MacArthur-Bates Communicative Developmental Inventories Toddler Form (Taiwan version). Additionally, participants' receptive and expressive language abilities were assessed using the receptive and expressive language subscales of the Bayley Scales of Infant and Toddler Development, Third Edition. At age 4, the Child Language Disorder Scale-Revised was applied and included the two core subtests for auditory comprehension and expressive communication. At ages 2 and 4 years, behavior problems were assessed with the Child Behavior Checklist. RESULTS: There was a higher percentage of participants with persistent behavior problems among LT toddlers than among TLD toddlers. Moreover, toddlers with larger vocabularies were less likely to develop withdrawal behaviors by preschool age. CONCLUSIONS: This study supported the temporal stability of parent-reported behavior problems among LT toddlers across early childhood. Early identification of and intervention for behavior problems associated with LT in toddlerhood is essential to alleviate their behavior problems later in preschool years.


Assuntos
Transtornos do Desenvolvimento da Linguagem , Estudos de Casos e Controles , Pré-Escolar , Humanos , Lactente , Desenvolvimento da Linguagem , Transtornos do Desenvolvimento da Linguagem/etiologia , Pais , Vocabulário
11.
Distúrb. comun ; 34(1): e55291, mar. 2022. tab
Artigo em Português | LILACS | ID: biblio-1396614

RESUMO

Objetivo: Analisar relação entre sofrimento psíquico e atraso na aquisição da linguagem. Método: uma amostra de 101 bebês, acompanhados dos três aos 24 meses por meio de filmagens das interações com suas mães, foram avaliados por protocolos de avaliação do psiquismo (Sinais PREAUT, roteiro IRDI e MCHAT) e pelos sinais enunciativos de aquisição da linguagem (SEAL). Os dados foram analisados estatisticamente por meio do teste de correlação de Pearson. Resultados: Observou-se maior correlação entre o roteiro IRDI, os Sinais PREAUT no primeiro semestre de vida. No segundo, terceiro e quarto semestre de vida dos bebês, o risco psíquico e o atraso na aquisição da linguagem coincidem, mas também há casos de atraso na aquisição da linguagem sem risco psíquico. Conclusão: Houve relação significativa entre presença de sofrimento psíquico e atraso na aquisição da linguagem.


Objective: To analyze the relationship between psychic distress and language acquisition delay. Method: a sample of 101 babies, followed from three to 24 months of age through videotaping of interactions with their mothers, were evaluated by psychic protocols (PREAUT signs, IRDI and MCHAT script) and by the enunciative signs of language acquisition (SEAL). Data were analyzed using the STATISTICA 9.0 software. Results: There was a greater correlation between the IRDI script and the PREAUT signs in the first semester of life. In the second, third and fourth semester of life, the psychic risk and the delay in language acquisition coincide, but there are cases of delay in the acquisition of language without psychic risk. Conclusion: There was a significant relationship between the presence of psychic distress and language acquisition delay.


Objetivo: Analizar la relación entre sufrimiento psíquico y retraso en la adquisición del lenguaje. Método: una muestra de 101 bebés, seguidos desde los 3 a los 24 meses de edad mediante videograbación de interacciones con sus madres, fueron evaluados mediante protocolos de riesgo psíquico (signos PREAUT, guión IRDI y MCHAT) y mediante los signos enunciativos de adquisición del lenguaje (SEAL) . Los datos se analizaron con el software STATISTICA 9.0. Resultados: Hubo una mayor correlación entre el guión IRDI y los signos PREAUT en el primer semestre de vida. En el segundo, tercer y cuarto semestre de vida, el riesgo psíquico y el retraso en la adquisición del lenguaje coinciden, pero existen casos de retraso en la adquisición del lenguaje sin riesgo psíquico. Conclusión: hubo una relación significativa entre la presencia de sufriemento psíquico y el retraso en la adquisición del lenguaje.


Assuntos
Humanos , Masculino , Feminino , Lactente , Angústia Psicológica , Transtornos do Desenvolvimento da Linguagem/etiologia , Estudos Retrospectivos , Estudos Longitudinais , Desenvolvimento da Linguagem , Relações Mãe-Filho
12.
Ital J Pediatr ; 47(1): 223, 2021 Nov 06.
Artigo em Inglês | MEDLINE | ID: mdl-34742324

RESUMO

Television studies have shown that some negative effects of screens could depend on exposure time, but more importantly on the characteristics of the child, the type of content viewed, and the context in which it is viewed. Studies on newer screens show that these factors are still valid but new ones now play a negative role: portable screens increase the duration of exposure and lowered the age at which exposure begins. More worryingly, new screen persuasive designs and dark patterns largely used incite more frequent use, attracting the attention of children and parents, resultantly interfering deeply in parent/child relationships. In this text we suggest that current academic recommendations have to be more broadly shared but also that new recommendations are needed: especially to advise parents not to let their screen interactions compete with real interactions with their child which are the core of learnings (especially language) and emotional regulations but also of their security.


Assuntos
Desenvolvimento Infantil , Cognição , Televisão , Criança , Transtornos do Comportamento Infantil/etiologia , Computadores de Mão , Relações Familiares , Humanos , Transtornos do Desenvolvimento da Linguagem/etiologia , Transtornos do Sono-Vigília/etiologia
13.
Rev Neurol ; 73(11): 394-400, 2021 Dec 01.
Artigo em Espanhol | MEDLINE | ID: mdl-34826333

RESUMO

INTRODUCTION: From a neuroconstructivism perspective, subtle atypicalities in low-level processes have a cascading impact on the domains for which these processes are relevant. Atypicalities in a given process contribute to accounting for the phenotype of different developmental disorders. According to current classification criteria, language disorders can occur in different developmental conditions. The temporal sampling theory has been proposed as a framework for such disorders. In this work, this theory is reviewed and analyzed from the aforementioned neuroconstructivism claims. DEVELOPMENT: The temporal sampling theory explains how atypicalities in the perception of the rise time acoustic parameter in the slowest temporal window of the auditory signal and, linked to this, potential atypicalities in the entrainment of the signal and the neural oscillations in the auditory cortex involve difficulties for language and music development. These atypicalities are linked to a different experience with the stimuli. In turn, the different experience derives from differences in rise time discrimination thresholds and in the received input that is related to this parameter. CONCLUSIONS: The temporal sampling theory offers an explanation that is consistent with the neuroconstructivism perspective. There is evidence of rise time perception difficulties and their relationship with language and music in children with developmental language disorder and/or dyslexia. Future studies should analyze the reach of this theory to explain language disorders in different developmental conditions.


TITLE: La teoría del muestreo temporal aplicada a los trastornos del lenguaje: análisis desde una perspectiva neuroconstructivista.Introducción. De acuerdo con una perspectiva neuroconstructivista, la existencia de atipicidades sutiles en procesos de bajo nivel tiene un impacto en cascada sobre los dominios para los que tales procesos son relevantes. Diferentes alteraciones en un mismo proceso pueden dar cuenta del fenotipo de trastornos distintos. Según los criterios clasificatorios actuales, los trastornos del lenguaje pueden estar presentes en distintas condiciones evolutivas. La teoría del muestreo temporal se ha propuesto como posible marco explicativo de dichos trastornos. En este trabajo se revisa esta teoría, aplicando para ello los postulados neuroconstructivistas mencionados. Desarrollo. La teoría del muestreo temporal plantea cómo alteraciones en la percepción del parámetro acústico del tiempo de ascenso de la amplitud en la ventana temporal lenta de la señal auditiva y, ligado a ello, posibles alteraciones en el acoplamiento entre dicha señal y las oscilaciones neurales de la corteza auditiva acarrean dificultades para el desarrollo lingüístico y musical. Tales alteraciones se vinculan a experiencias distintas con la información estimular, derivadas de diferencias en los umbrales de discriminación del tiempo de ascenso de la amplitud y en el input recibido asociado a este parámetro. Conclusiones. La teoría analizada ofrece una explicación consistente con el marco neuroconstructivista. Existe evidencia acerca de las dificultades perceptivas del tiempo de ascenso de la amplitud y su relación con los dominios lingüístico y musical en niños con trastorno del desarrollo del lenguaje y/o con dislexia. Estudios futuros deberían analizar el alcance de esta teoría para explicar los trastornos del lenguaje en otras condiciones evolutivas.


Assuntos
Transtornos do Desenvolvimento da Linguagem , Criança , Humanos , Desenvolvimento da Linguagem , Transtornos do Desenvolvimento da Linguagem/etiologia , Teoria de Sistemas , Fatores de Tempo
15.
PLoS Med ; 18(9): e1003701, 2021 09.
Artigo em Inglês | MEDLINE | ID: mdl-34582452

RESUMO

BACKGROUND: Annually 125 million pregnancies are at risk of malaria infection. However, the impact of exposure to malaria in pregnancy on neurodevelopment in children is not well understood. We hypothesized that malaria in pregnancy and associated maternal immune activation result in neurodevelopmental delay in exposed offspring. METHODS AND FINDINGS: Between April 2014 and April 2015, we followed 421 Malawian mother-baby dyads (median [IQR] maternal age: 21 [19, 28] years) who were previously enrolled (median [IQR] gestational age at enrollment: 19.7 [17.9, 22.1] weeks) in a randomized controlled malaria prevention trial with 5 or 6 scheduled assessments of antenatal malaria infection by PCR. Children were evaluated at 12, 18, and/or 24 months of age with cognitive tests previously validated in Malawi: the Malawi Developmental Assessment Tool (MDAT) and the MacArthur-Bates Communicative Development Inventories (MCAB-CDI). We assessed the impact of antenatal malaria (n [%] positive: 240 [57.3]), placental malaria (n [%] positive: 112 [29.6]), and maternal immune activation on neurocognitive development in children. Linear mixed-effects analysis showed that children exposed to antenatal malaria between 33 and 37 weeks gestation had delayed language development across the 2-year follow-up, as measured by MCAB-CDI (adjusted beta estimate [95% CI], -7.53 [-13.04, -2.02], p = 0.008). Maternal immune activation, characterized by increased maternal sTNFRII concentration, between 33 and 37 weeks was associated with lower MCAB-CDI language score (adjusted beta estimate [95% CI], -8.57 [-13.09, -4.06], p < 0.001). Main limitations of this study include a relatively short length of follow-up and a potential for residual confounding that is characteristic of observational studies. CONCLUSIONS: This mother-baby cohort presents evidence of a relationship between malaria in pregnancy and neurodevelopmental delay in offspring. Malaria in pregnancy may be a modifiable risk factor for neurodevelopmental injury independent of birth weight or prematurity. Successful interventions to prevent malaria during pregnancy may reduce the risk of neurocognitive delay in children.


Assuntos
Transtornos do Desenvolvimento da Linguagem/etiologia , Malária/fisiopatologia , Transtornos Neurocognitivos/etiologia , Complicações Infecciosas na Gravidez , Estudos de Coortes , Feminino , Humanos , Lactente , Transmissão Vertical de Doenças Infecciosas , Malária/embriologia , Malária/imunologia , Malaui , Masculino , Transtornos Neurocognitivos/prevenção & controle , Testes Neuropsicológicos , Gravidez , Complicações Infecciosas na Gravidez/imunologia
16.
JAMA Netw Open ; 4(8): e2122591, 2021 08 02.
Artigo em Inglês | MEDLINE | ID: mdl-34432009

RESUMO

Importance: Pediatric single-sided deafness (SSD) can seriously affect development, causing impaired spatial hearing skills, speech-language delays, and academic underachievement. Early cochlear implantation likely improves hearing-related outcomes, but its association with language development remains unclear. Objective: To investigate whether early cochlear implantation is associated with language outcomes for children with prelingual SSD. Design, Setting, and Participants: The Cochlear Implant for Children and One Deaf Ear study was initiated in 2015 and recruited participants at 4 academic hospitals in Flanders, Belgium, through 2019. This cohort study included 3 groups of children aged 2 to 5 years: children with SSD and a cochlear implant, children with SSD without a cochlear implant, and a control group with normal hearing. Language and hearing skills were assessed 1 to 2 times per year until the age of 10 years. Study completion rates were high (82%). Data analysis was performed from October to December 2020. Exposure: Unilateral cochlear implant. Main Outcomes and Measures: Longitudinal vocabulary, grammar, and receptive language scores. The implanted group was hypothesized to outperform the nonimplanted group on all language tests. Results: During the recruitment period, 47 children with prelingual SSD without additional disabilities were identified at the participating hospitals. Fifteen of the 34 children with an intact auditory nerve received a cochlear implant (44%, convenience sample). Sixteen of the remaining children were enrolled in the SSD control group (50%). Data from 61 children (mean [SD] age at the time of enrollment, 2.08 [1.34] years; 26 girls [42%]) were included in the analysis: 15 children with SSD and a cochlear implant, 16 children with SSD without a cochlear implant, and 30 children with normal hearing. Children with SSD and a cochlear implant performed in line with their peers with normal hearing with regard to grammar. In contrast, children with SSD without a cochlear implant had worse grammar scores than the group with implants (-0.76; 95% CI, -0.31 to -1.21; P = .004) and the group with normal hearing (-0.53; 95% CI, -0.91 to -0.15; P = .02). The 3 groups had similar vocabulary and receptive language abilities. Conclusions and Relevance: These findings suggest that early cochlear implantation is associated with normal grammar development in young children with prelingual SSD. Although further follow-up will reveal the long-term outcomes of the cochlear implant for other skills, the current results will help clinicians and policy makers identify the best treatment option for these children.


Assuntos
Implante Coclear/métodos , Surdez/complicações , Surdez/cirurgia , Diagnóstico Precoce , Transtornos do Desenvolvimento da Linguagem/etiologia , Transtornos do Desenvolvimento da Linguagem/prevenção & controle , Desenvolvimento da Linguagem , Bélgica , Criança , Pré-Escolar , Estudos de Coortes , Feminino , Humanos , Estudos Longitudinais , Masculino
18.
Neuropsychologia ; 158: 107907, 2021 07 30.
Artigo em Inglês | MEDLINE | ID: mdl-34058175

RESUMO

Language difficulties of children with Developmental Language Disorder (DLD) have been associated with multiple underlying factors and are still poorly understood. One way of investigating the mechanisms of DLD language problems is to compare language-related brain activation patterns of children with DLD to those of a population with similar language difficulties and a uniform etiology. Children with 22q11.2 deletion syndrome (22q11DS) constitute such a population. Here, we conducted an fMRI study, in which children (6-10yo) with DLD and 22q11DS listened to speech alternated with reversed speech. We compared language laterality and language-related brain activation levels with those of typically developing (TD) children who performed the same task. The data revealed no significant differences between groups in language lateralization, but task-related activation levels were lower in children with language impairment than in TD children in several nodes of the language network. We conclude that language impairment in children with DLD and in children with 22q11DS may involve (partially) overlapping cortical areas.


Assuntos
Síndrome de DiGeorge , Transtornos do Desenvolvimento da Linguagem , Encéfalo/diagnóstico por imagem , Criança , Linguagem Infantil , Síndrome de DiGeorge/complicações , Síndrome de DiGeorge/diagnóstico por imagem , Humanos , Transtornos do Desenvolvimento da Linguagem/etiologia , Fala
19.
Am J Hum Genet ; 108(6): 1138-1150, 2021 06 03.
Artigo em Inglês | MEDLINE | ID: mdl-33909992

RESUMO

ANKRD17 is an ankyrin repeat-containing protein thought to play a role in cell cycle progression, whose ortholog in Drosophila functions in the Hippo pathway as a co-factor of Yorkie. Here, we delineate a neurodevelopmental disorder caused by de novo heterozygous ANKRD17 variants. The mutational spectrum of this cohort of 34 individuals from 32 families is highly suggestive of haploinsufficiency as the underlying mechanism of disease, with 21 truncating or essential splice site variants, 9 missense variants, 1 in-frame insertion-deletion, and 1 microdeletion (1.16 Mb). Consequently, our data indicate that loss of ANKRD17 is likely the main cause of phenotypes previously associated with large multi-gene chromosomal aberrations of the 4q13.3 region. Protein modeling suggests that most of the missense variants disrupt the stability of the ankyrin repeats through alteration of core structural residues. The major phenotypic characteristic of our cohort is a variable degree of developmental delay/intellectual disability, particularly affecting speech, while additional features include growth failure, feeding difficulties, non-specific MRI abnormalities, epilepsy and/or abnormal EEG, predisposition to recurrent infections (mostly bacterial), ophthalmological abnormalities, gait/balance disturbance, and joint hypermobility. Moreover, many individuals shared similar dysmorphic facial features. Analysis of single-cell RNA-seq data from the developing human telencephalon indicated ANKRD17 expression at multiple stages of neurogenesis, adding further evidence to the assertion that damaging ANKRD17 variants cause a neurodevelopmental disorder.


Assuntos
Anormalidades Craniofaciais/etiologia , Heterozigoto , Deficiência Intelectual/etiologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Mutação com Perda de Função , Proteínas de Ligação a RNA/genética , Adolescente , Adulto , Criança , Pré-Escolar , Anormalidades Craniofaciais/patologia , Feminino , Haploinsuficiência , Humanos , Lactente , Deficiência Intelectual/patologia , Transtornos do Desenvolvimento da Linguagem/patologia , Masculino , Linhagem , Fenótipo , Proteínas de Ligação a RNA/metabolismo , Transdução de Sinais , Síndrome , Adulto Jovem
20.
Matern Child Health J ; 25(6): 900-908, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-33905063

RESUMO

INTRODUCTION: From the ecological perspective of multifactorial causal mechanism, the communicative interaction environment has been less studied in early childhood which is the most sensitive phase for language development. We aimed to research simultaneous communicative environmental factors including maternal depression and media usage patterns in young children aged 1-31/2 years. METHODS: One hundred and one participants were included in the study; fifty-one children with language delay as the case group and fifty children with typical development as the control group. Maternal depressive symptoms were evaluated by Beck Depression Inventory. The general development of each child was evaluated by Denver II Screening Test and Bayley-Third Edition. Language development was evaluated by the Preschool Language Scale-5. The questionnaire for the sociodemographic data and media usage patterns was prepared by the study team. RESULTS: Maternal depression scores, duration of TV viewing, background TV were higher in the children with language delay and they started earlier using screen devices in comparison with the control group (p < 0.05). The total amount of interaction time and co-viewing were less in children with language delay and more parents intended to keep their children occupied by watching in the case group (p < 0.05). Mother care-giving (p = 0.002, OR = 5.80, CI 1.93-17.4) and absence of co-viewing (p = 0.000, OR = 9.46, CI 2.69-33.3) were the significant factors associated with language delay. DISCUSSION: Young children with language delay were more exposed to communicative environmental risk factors than children with typical development. The integration of this perspective to child health care practices should be encouraged in early childhood.


Assuntos
Depressão , Transtornos do Desenvolvimento da Linguagem , Desenvolvimento da Linguagem , Criança , Pré-Escolar , Depressão/epidemiologia , Depressão/etiologia , Humanos , Lactente , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Transtornos do Desenvolvimento da Linguagem/epidemiologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Relações Mãe-Filho , Pais , Inquéritos e Questionários
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