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1.
Mol Genet Metab ; 102(2): 153-6, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21144783

RESUMO

We describe the clinical and molecular features of a child harboring a novel mutation in SLC6A8 gene in association with a milder phenotype than other creatine transporter (CT1) deficient patients (OMIM 300352) [1-7]. The mutation c.757 G>C p.G253R in exon 4 of SLC6A8 was hemizygous in the child, aged 6 years and 6 months, who showed mild intellectual disability with severe speech and language delay. His carrier mother had borderline intellectual functioning. Although the neurochemical and biochemical parameters were fully consistent with those reported in the literature for subjects with CT1 deficit, in our patient within a general cognitive disability, a discrepancy between nonverbal and verbal skills was observed, confirming the peculiar vulnerability of language development under brain Cr depletion.


Assuntos
Deficiência Intelectual/genética , Transtornos da Linguagem/genética , Proteínas de Membrana Transportadoras/genética , Mutação , Adulto , Sequência de Bases , Criança , Feminino , Humanos , Deficiência Intelectual/diagnóstico , Transtornos da Linguagem/diagnóstico , Masculino , Dados de Sequência Molecular , Alinhamento de Sequência
2.
Res Dev Disabil ; 89: 59-68, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30947105

RESUMO

BACKGROUND: In spite of the large literature on Late Talkers (LTs) it's still unclear which factors predict outcome in children younger than 3 years old. AIMS: To identify the early language characteristics of LTs whose outcome was either a transient delay or a Developmental Language Disorder (DLD). METHODS AND PROCEDURES: 50 LTs were assessed both by indirect and direct measures of expressive and receptive language at three time points between 2 and 4 years of age. OUTCOMES AND RESULTS: At the first evaluation, all LTs had an expressive language delay; 61% also had delayed early syntactic comprehension. Three different linguistic outcomes emerged: children who caught up with their peers ("Late Bloomers") at age 3; children with slow language recovery ("Slow Learners") at age 4 and children at risk of DLD. The linguistic measures that differentiated the groups changed with age. By 28 months, impaired syntactic comprehension differentiated children at risk of DLD at 4 years of age, from the other two groups. By 36 months, the discrepancy between vocabulary size and age was larger in children with persistent language difficulties compared to both "Late Bloomers" and "Slow Learners". Expressive grammar differentiated the groups significantly by age 3 with difficulties in this domain still persisting in children with DLD at age 4. CONCLUSIONS: An early syntactic comprehension delay was a predictive index of DLD in LTs, suggesting the importance of evaluating this language component when assessing LT toddlers. IMPLICATIONS: LTs with receptive-expressive language delay around 24-30 months could benefit from an early language intervention.


Assuntos
Compreensão , Transtornos do Desenvolvimento da Linguagem , Desenvolvimento da Linguagem , Testes de Linguagem , Fala , Pré-Escolar , Feminino , Humanos , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Transtornos do Desenvolvimento da Linguagem/psicologia , Linguística , Masculino , Valor Preditivo dos Testes , Prognóstico , Comportamento Verbal
3.
Cortex ; 36(1): 31-46, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10728895

RESUMO

Although some studies have reported subtle language deficits following early focal brain lesions (EFBL), most studies find no evidence for differential language outcomes as a function of lesion side or lesion type in children with congenital injuries to one side of the brain. However, recent prospective studies of the first stages of language development in English-speaking children with EFBL have reported greater delays in expressive vocabulary in children with left-hemisphere damage, particularly if the lesion involves left temporal cortex. In the present study, first stages in the development of word production were studied in 43 Italian children with congenital EFBL, between 13 and 46 months of age. As a group, the EFBL children were markedly delayed in expressive vocabulary. Among children who were in the first stage of language learning, delays were significantly greater with left-hemisphere injury. However, this left-right difference was not evident in children who had moved on to the next stage of language development, producing at least some sentences. Discussion centers on the role of developmental plasticity in determining the outcomes of early focal brain injury, suggesting that recovery from initial delays may take place in the early stages of language development, at least for some children.


Assuntos
Lesões Encefálicas/fisiopatologia , Lesões Encefálicas/psicologia , Encéfalo/fisiopatologia , Desenvolvimento Infantil , Desenvolvimento da Linguagem , Plasticidade Neuronal/fisiologia , Pré-Escolar , Feminino , Humanos , Lactente , Masculino
4.
J Child Neurol ; 16(5): 309-16, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11392514

RESUMO

Early cognitive and language development of children with congenital focal brain lesions, documented by magnetic resonance imaging, was studied in 18 cases, 9 with left-hemisphere damage and 9 with right-hemisphere damage, at about 2 (Time 1) and 4 years of age (Time 2). All of the children showed normal cognitive development, but their global Griffiths Developmental Scales scores were lower at Time 2, and developmental profiles across individual subscales revealed side-specific effects, resembling the adult left/right cerebral hemisphere lesion model. Expressive lexicon and grammar were delayed, more often in left-hemisphere-damaged than in right-hemisphere-damaged children, at Time 1 and Time 2. Functional findings were not related to the size and location of the brain lesion, whereas the presence of epilepsy was a highly significant predictor of cognitive and language outcome, irrespective of the side of the lesion. The stable disadvantage in the verbal domain shown by left-hemisphere-damaged children within the age range of this study might suggest that the left hemisphere has some initial bias for language learning. The effects of right-hemisphere damage were more variable and emerged at a later stage of language development.


Assuntos
Encéfalo/patologia , Encéfalo/fisiopatologia , Transtornos Cognitivos/etiologia , Deficiências do Desenvolvimento/etiologia , Epilepsia/complicações , Epilepsia/fisiopatologia , Transtornos do Desenvolvimento da Linguagem/etiologia , Fatores Etários , Pré-Escolar , Transtornos Cognitivos/diagnóstico , Deficiências do Desenvolvimento/diagnóstico , Feminino , Lateralidade Funcional/fisiologia , Humanos , Lactente , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Testes de Linguagem , Imageamento por Ressonância Magnética , Masculino , Testes Neuropsicológicos , Índice de Gravidade de Doença
5.
Brain Lang ; 77(3): 283-93, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11386697

RESUMO

The paper presents a comparison of the development of the Italian determiner system in three different populations: normally developing children, a child recovering from childhood aphasia from the age of 3 years, 9 months, and 11 specific language impairment (SLI) children. Data from Italian normal children provide evidence for the hypothesis (1) that no prefunctional stage exists as far as the determiner system is concerned and (2) that the syntactic properties of determiners play an essential triggering role early on. The analysis of the determiner system in the aphasic child has a double interest. On the one hand, it may help to shed light on some of the intriguing questions concerning this type of disorder; on the other, it may be relevant for the discussion of the notion of agrammatism. Results of the morphosyntactic analysis reveal that, apart from timing differences, recovery from childhood aphasia shares important features with normal development. Differently from mean length of utterance (MLU)-matched normal controls and the aphasic child, SLI children omit determiners significantly more often than almost any other functional category or free morpheme. We will argue that the reasons for the SLI children's atypical behavior have to be sought in the nonaccessibility to or in the misappreciation of one fundamental syntactic property of determiners: their role as elements that assign argumenthood to nominal expressions (Szabolcsi, 1987; Longobardi, 1994).


Assuntos
Afasia/diagnóstico , Transtornos da Linguagem/diagnóstico , Idioma , Aprendizagem Verbal , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Índice de Gravidade de Doença
6.
Percept Mot Skills ; 59(3): 1007-10, 1984 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-6522185

RESUMO

Evidence for normal development of linguistic but poor visuo-perceptual skills has been obtained with the neuropsychological assessment of a case of early left-brain injury. Data suggest the transfer of linguistic functions from the left to the right hemisphere at the expense of visuo-perceptual capacities for which the right hemisphere is potentially specialized.


Assuntos
Dano Encefálico Crônico/congênito , Dominância Cerebral , Hemiplegia/congênito , Testes Neuropsicológicos , Atrofia , Dano Encefálico Crônico/psicologia , Córtex Cerebral/patologia , Criança , Dominância Cerebral/fisiologia , Hemiplegia/psicologia , Humanos , Desenvolvimento da Linguagem , Masculino , Percepção Visual/fisiologia , Escalas de Wechsler
7.
Minerva Pediatr ; 64(2): 213-23, 2012 Apr.
Artigo em Italiano | MEDLINE | ID: mdl-22495195

RESUMO

AIM: Sensorineural hearing loss (SNHL) is complicated by additional disabilities in about 30% of cases, but the epidemiology of associated disorders, in terms of type, frequency and aetiology is still not clearly defined. Additional disabilities in a deaf child have important consequences in assessing and choosing a therapeutic treatment, in particular when considering cochlear implantation (CI) or hearing aids (HA). The aim of this paper was to evaluate frequency, type and severity of additional neurodevelopmental disabilities in children with profound bilateral sensorineural hearing loss and to investigate the relationship between disability and the etiology of deafness. METHODS: Eighty children with profound bilateral sensorineural hearing loss (mean age 5.4 years) were investigated by means of a diagnostic protocol including clinical, neurodevelopmental, and audiological procedures together with genetic and neurometabolic tests and neuroradiological investigation by brain MRI. RESULTS: Fifty-five percent of the sample exhibited one or more disabilities in addition to deafness, with cognitive, behavioural-emotional and motor disorders being the most frequent. The risk of additional disabilities varied according to aetiology, with a higher incidence in hereditary syndromic deafness, in cases due to pre-perinatal pathology (in comparison to unknown and hereditary non syndromic forms) and in the presence of major brain abnormalities at MRI. CONCLUSION: Our results suggest that the aetiology of deafness may be a significant risk indicator for the presence of neuropsychiatric disorders. A multidimensional evaluation, including aetiological, neurodevelopmental and MRI investigation is needed for formulating prognosis and for planning therapeutic intervention, especially in those children candidated to cochlear implant.


Assuntos
Surdez/diagnóstico , Surdez/etiologia , Deficiências do Desenvolvimento/complicações , Deficiências do Desenvolvimento/diagnóstico , Perda Auditiva Neurossensorial/diagnóstico , Perda Auditiva Neurossensorial/etiologia , Testes Neuropsicológicos , Adolescente , Criança , Pré-Escolar , Implante Coclear , Surdez/complicações , Surdez/epidemiologia , Surdez/terapia , Deficiências do Desenvolvimento/epidemiologia , Feminino , Auxiliares de Audição , Perda Auditiva Neurossensorial/complicações , Perda Auditiva Neurossensorial/epidemiologia , Perda Auditiva Neurossensorial/terapia , Humanos , Incidência , Lactente , Itália/epidemiologia , Imageamento por Ressonância Magnética , Masculino , Valor Preditivo dos Testes , Prevalência , Estudos de Amostragem , Sensibilidade e Especificidade , Índice de Gravidade de Doença , Resultado do Tratamento
8.
Brain Lang ; 106(3): 211-25, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18267339

RESUMO

In the present paper, we address brain-behaviour relationships in children with acquired aphasia, by reviewing some recent studies on the effects of focal brain lesions on language development. Timing of the lesion, in terms of its occurrence, before or after the onset of speech and language acquisition, may be a major factor determining language outcome. However, it is still unclear which are the effects of aphasia occurring between 2 and 5 years of age, a time window which is crucial for acquiring and automatizing the basic rules of native language. A comprehensive review of the literature on acquired childhood aphasia precedes the description of long-term follow-up (20 years) of two identical twins, one of whom became aphasic at 3 years and 4 months after infarction of the left sylvian artery. Psycholinguistic analysis and fMRI data show a slow and incomplete recovery from non-fluent aphasia associated to an intra-hemispheric organization of language. These data, which support the potential but also the limits of neural plasticity during language development, are discussed in the light of the literature on the time-course and neural bases of acquired childhood aphasia.


Assuntos
Afasia/fisiopatologia , Encefalopatias/fisiopatologia , Infarto Cerebral/fisiopatologia , Desenvolvimento da Linguagem , Afasia/etiologia , Afasia/patologia , Encefalopatias/etiologia , Encefalopatias/patologia , Infarto Cerebral/complicações , Infarto Cerebral/patologia , Pré-Escolar , Período Crítico Psicológico , Seguimentos , Humanos , Imageamento por Ressonância Magnética , Masculino , Plasticidade Neuronal/fisiologia , Recuperação de Função Fisiológica/fisiologia , Literatura de Revisão como Assunto , Fala/fisiologia
9.
Dev Med Child Neurol ; 47(11): 725-30, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16225734

RESUMO

The effects of congenital, unilateral, focal brain lesions on early linguistic development and hemispheric lateralization for language were investigated longitudinally in 24 preschool children with hemiplegia (14 males, 10 females), 12 with left hemisphere damage (LHD) and 12 with right hemisphere damage (RHD). A comprehensive linguistic assessment was performed at 2 and 3 years of life; cerebral lateralization for language was measured by the Fused Dichotic Words Listening Test. An early left-side specificity for language was indicated by the presence of lexical and grammatical delay in most children with LHD. In the dichotic listening test all 12 children with LHD showed a shift of language lateralization from the left to the right hemisphere. Atypical lateralization coefficients (lambda), i.e. values falling more than two standard deviations from the mean of a normative sample, were associated with a delay in lexical and grammatical development, especially after LHD. In addition, cortical-subcortical-periventricular lesions rather than solely periventricular damage, and larger lesions rather than small, were associated with the most atypical lateralization coefficients, irrespective of lesion side. Results of this study suggest that language and lateralization data are closely related and that reallocation of language functions in alternative regions of the brain has a cost in terms of a slow rate of language acquisition.


Assuntos
Encefalopatias/complicações , Hemiplegia/complicações , Desenvolvimento da Linguagem , Pré-Escolar , Feminino , Lateralidade Funcional , Humanos , Lactente , Linguística , Estudos Longitudinais , Masculino
10.
Int J Lang Commun Disord ; 33(3): 245-80, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-10326040

RESUMO

Most of the literature on children with specific language impairment (SLI) is centred on the study of cross-sectional samples and little is known on how language develops in these children--that is, whether it occurs along steps and modes analogous to those observed in normal acquisition, the only difference being significant slowness, or following rather idiosyncratic courses leading to atypical results. This paper presents findings from a longitudinal study of the acquisition of formal aspects of Italian grammar in a child with severe SLI of the so-called phonologic-syntactic subtype or grammatical SLI. The analysis concerns a set of morphosyntactic phenomena sufficiently differentiated in terms of both grammatical properties and modes of acquisition in normal development, so as to offer a panorama that approximates to what can be thought of as an overall morphosyntactic competence: (1) free morphology (prepositions, clitics and articles); (2) bound morphology (verb inflection); (3) WH movement (questions and relative clauses) and (4) the evolution of complex sentences. These phenomena will be dealt with in four independent studies. This paper argues that each domain or even each sub-domain presents its own set of properties, some of which are common to other domains but some of which are not. The results reveal the existence of important dissociations among the various domains and even within specific sub-domains. These dissociations may be ascribed to deficits affecting specific properties of functors or constructions. The picture that emerges is one in which the deficit involves, rather than morphology in the strict sense of a bare set of paradigmatic forms, some properties or components of syntax which are involved in the use, not only of certain morphemes, but of certain extended syntactic constructions as well. This result will be checked against the most widely held current theoretical approaches to SLI.


Assuntos
Afasia/psicologia , Desenvolvimento da Linguagem , Fatores Etários , Criança , Seguimentos , Humanos , Masculino , Semântica
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