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1.
Epilepsy Behav ; 55: 6-10, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26720703

RESUMO

Impairments in executive skills broadly span across multiple childhood epilepsy syndromes and can adversely affect quality of life. Bilingualism has been previously shown to correlate with enhanced executive functioning in healthy individuals. This study sought to determine whether the bilingual advantage in executive functioning exists in the context of pediatric epilepsy. We retrospectively analyzed neuropsychological data in 52 children with epilepsy and compared executive function scores in monolingual versus bilingual children with epilepsy while controlling for socioeconomic status and ethnicity. Bilingual children performed significantly better on the Working Memory Index than did monolingual children. There were no significant differences on the remaining executive function variables. The bilingual advantage appears to persist for working memory in children with epilepsy. These findings suggest that bilingualism is potentially a protective variable in the face of epilepsy-related working memory dysfunction.


Assuntos
Epilepsia/psicologia , Memória de Curto Prazo , Multilinguismo , Adolescente , Criança , Etnicidade , Função Executiva , Feminino , Humanos , Masculino , Testes Neuropsicológicos , Estudos Retrospectivos , Fatores Socioeconômicos , Teste de Sequência Alfanumérica , Escalas de Wechsler
2.
J Child Neurol ; 29(3): 318-25, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23358628

RESUMO

This study utilized diffusion tensor imaging fiber tractography to examine the miscrostructural integrity of limbic and paralimbic white matter tracts in 36 children (age M = 124 months) with histories of early deprivation, raised from birth in orphanages and subsequently adopted into the United States, compared to 16 age-matched typically developing children. We found increased mean diffusivity bilaterally in the arcuate fasciculus and increased mean diffusivity and reduced fractional anisotropy bilaterally in the uncinate fasciculus and cingulum in children with early deprivation. Microstructural integrity of the left arcuate fasciculus and right cingulum was related to language and behavioral functioning, respectively. White matter abnormalities were also associated with length of deprivation and time in the adoptive home. Our findings suggest that white matter pathways, connecting limbic and paralimbic brain regions is abnormal in children with histories of early deprivation, with some pathways appearing more susceptible to early deprivation than others.


Assuntos
Encéfalo/anormalidades , Idioma , Sistema Límbico/anormalidades , Orfanatos , Adoção , Anisotropia , Criança , Pré-Escolar , Imagem de Tensor de Difusão , Relações Familiares , Feminino , Humanos , Lactente , Recém-Nascido , Testes de Linguagem , Masculino , Fibras Nervosas Mielinizadas , Vias Neurais/anormalidades , Testes Neuropsicológicos , Carência Psicossocial , Fatores de Tempo
3.
J Clin Psychol Med Settings ; 21(1): 72-80, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24158241

RESUMO

The research objective was to identify the factor structure of the pediatric symptom checklist (PSC) in children with voiding dysfunction and/or nocturnal enuresis who were seen in a pediatric urology clinic. Retrospective chart reviews were conducted for 498 consecutive patients, ages 6-16, who were seen over a 13-month period. The PSC, a 35-item measure used to screen for psychosocial difficulties, was completed by the patient's caregiver. Confirmatory factor analyses using three previous models were conducted. A four factor model comprised of internalizing, externalizing, attention problems, and chronic illness factors represented the best fit to the data. Within this population, the PSC appears to capture internalizing and externalizing problems, difficulties with attention, and possible side effects of a medical condition. This information could aid clinicians in assessing adjustment difficulties within this population and concurrently allow researchers to examine whether these specific factors are related to other relevant outcomes.


Assuntos
Lista de Checagem/métodos , Lista de Checagem/normas , Enurese/diagnóstico , Transtornos Mentais/diagnóstico , Pediatria/métodos , Adolescente , Lista de Checagem/estatística & dados numéricos , Criança , Enurese/psicologia , Análise Fatorial , Feminino , Humanos , Masculino , Transtornos Mentais/complicações , Transtornos Mentais/psicologia , Enurese Noturna/complicações , Enurese Noturna/diagnóstico , Enurese Noturna/psicologia , Pediatria/estatística & dados numéricos , Estudos Retrospectivos , Inquéritos e Questionários
4.
Urology ; 80(4): 907-12, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23021666

RESUMO

OBJECTIVE: To assess rates of psychosocial difficulties in children seen in a pediatric urology clinic to determine whether all patients should be screened for psychosocial problems, and to use standardized measures to determine whether the severity of voiding dysfunction and/or enuresis in children is related to their degree of psychosocial difficulties. METHODS: A retrospective chart review was conducted to collect the Pediatric Symptom Checklist from all children referred to an outpatient urology clinic over a 6-month period. In addition, scores from the child's Dysfunctional Voiding Scoring System were collected for patients referred for voiding dysfunction and/or enuresis. RESULTS: Caregivers of 600 children completed the Pediatric Symptom Checklist as part of their child's outpatient clinic paperwork. Overall, 15.2% of the patients met the clinical cut-off for significant psychosocial difficulties. However, children with voiding dysfunction and/or enuresis were at increased risk for these problems, with the severity of their psychosocial difficulties being related to the severity of their urologic condition. CONCLUSION: It is unnecessary to screen all pediatric urology patients, although those referred for voiding dysfunction and/or enuresis should be screened for psychosocial difficulties. Children at greatest risk for psychosocial problems were those who were male, had a high body mass index, had nocturnal enuresis, had an elevated Dysfunctional Voiding Scoring System score, and/or reported frequent episodes of wetting or soaking their underwear when they wet. Importantly, children appear to be most concerned with "wetness."


Assuntos
Doenças dos Genitais Femininos/complicações , Doenças dos Genitais Masculinos/complicações , Nefropatias/complicações , Transtornos Mentais/complicações , Transtornos Urinários/psicologia , Anormalidades Urogenitais/complicações , Adolescente , Fatores Etários , Assistência Ambulatorial , Ansiedade/complicações , Transtorno do Deficit de Atenção com Hiperatividade/complicações , Índice de Massa Corporal , Criança , Pré-Escolar , Depressão/complicações , Feminino , Doenças dos Genitais Femininos/diagnóstico , Doenças dos Genitais Masculinos/diagnóstico , Humanos , Nefropatias/diagnóstico , Masculino , Análise Multivariada , Enurese Noturna/complicações , Enurese Noturna/diagnóstico , Enurese Noturna/psicologia , Razão de Chances , Estudos Retrospectivos , Índice de Gravidade de Doença , Inquéritos e Questionários , Transtornos Urinários/complicações , Transtornos Urinários/diagnóstico , Anormalidades Urogenitais/diagnóstico , Urologia
5.
J Pediatr ; 160(1): 147-51, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21839473

RESUMO

OBJECTIVE: To investigate whether abnormal regional white matter architecture in the perisylvian region could be used as an easy and sensitive quantitative method to demonstrate language pathway abnormalities in children with developmental delay (DD). STUDY DESIGN: We performed diffusion tensor imaging in 15 DD subjects (age, 61.1 ± 20.9 months) and 15 age-matched typically developing (TD) children (age, 68.4 ± 19.2 months). With diffusion tensor imaging color-coded orientation maps, we quantified the fraction of fibers in the perisylvian region that are oriented in anteroposterior (AP) and mediolateral (ML) directions, and their ratio (AP/ML) was calculated. RESULTS: The AP/ML ratio was more sensitive than tractography in characterizing perisylvian regional abnormalities in DD children. The AP/ML ratio of the left perisylvian region was significantly lower in DD children compared with TD children (P = .03). The ML component of bilateral perisylvian regions was significantly higher in DD children compared with TD children (P = .01 [left] and P = .004 [right]). No significant difference was found in the AP component in the two groups. A significant negative correlation of the left ML component with Vineland communication skills was observed (r = -0.657, P = .011). CONCLUSIONS: The AP/ML ratio appears to be a sensitive indicator of regional white matter architectural abnormalities in the perisylvian region of DD children.


Assuntos
Mapeamento Encefálico/métodos , Deficiências do Desenvolvimento/complicações , Imagem de Tensor de Difusão , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Transtornos do Desenvolvimento da Linguagem/etiologia , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Testes Neuropsicológicos , Sensibilidade e Especificidade
6.
J Child Neurol ; 27(1): 39-45, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21940690

RESUMO

The objective of this study is to determine the long-term outcome of children with intractable epilepsy who have diffuse cortical hypometabolism on 2-deoxy-2-((18)F)fluoro-D-glucose positron emission tomography (FDG-PET) scans. Seventeen children with intractable epilepsy showing bilateral, diffuse cortical hypometabolism on FDG-PET were followed up through telephone interview from 1 year 4 months to 11 years 4 months (mean: 5 years 7 months ± 2 years 1 month) after their PET scans. One child succumbed to Sanfilippo disease at age 20 years. Only 2 children were seizure free. Fifty percent had walking difficulties, 56.25% were not toilet trained, all had speech difficulties, 43.75% had behavioral problems, 37.5% had poor eye contact, 75% had socialization difficulties, and 87.5% attended special schools. Three children were found to have genetic causes, including a 4-MB deletion of the mitochondrial genome, MECP2 duplication, and Lafora disease. In conclusion, the long-term outcome in this patient population is poor, and they tend to suffer from genetic/neurodegenerative diseases.


Assuntos
Córtex Cerebral/diagnóstico por imagem , Deficiências do Desenvolvimento/diagnóstico por imagem , Epilepsia/patologia , Glucose/metabolismo , Tomografia por Emissão de Pósitrons , Adolescente , Mapeamento Encefálico , Criança , Pré-Escolar , Deficiências do Desenvolvimento/etiologia , Eletroencefalografia , Feminino , Fluordesoxiglucose F18 , Humanos , Lactente , Estudos Longitudinais , Imageamento por Ressonância Magnética , Masculino , Estudos Retrospectivos
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