Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
1.
Cereb Cortex ; 30(2): 587-596, 2020 03 21.
Artigo em Inglês | MEDLINE | ID: mdl-31216015

RESUMO

Turner syndrome (TS) is a genetic disorder affecting approximately 1:2000 live-born females. It results from partial or complete X monosomy and is associated with a range of clinical issues including a unique cognitive profile and increased risk for certain behavioral problems. Structural neuroimaging studies in adolescents, adults, and older children with TS have revealed altered neuroanatomy but are unable to identify when in development differences arise. In addition, older children and adults have often been exposed to years of growth hormone and/or exogenous estrogen therapy with potential implications for neurodevelopment. The study presented here is the first to test whether brain structure is altered in infants with TS. Twenty-six infants with TS received high-resolution structural MRI scans of the brain at 1 year of age and were compared to 47 typically developing female and 39 typically developing male infants. Results indicate that the typical neuroanatomical profile seen in older individuals with TS, characterized by decreased gray matter volumes in premotor, somatosensory, and parietal-occipital cortex, is already present at 1 year of age, suggesting a stable phenotype with origins in the prenatal or early postnatal period.


Assuntos
Encéfalo/patologia , Síndrome de Turner/patologia , Encéfalo/diagnóstico por imagem , Feminino , Humanos , Lactente , Imageamento por Ressonância Magnética , Tamanho do Órgão , Síndrome de Turner/diagnóstico por imagem
2.
J Intellect Disabil Res ; 63(10): 1234-1247, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31134691

RESUMO

BACKGROUND: Anxiety is considered a 'frequent' feature in the clinical criteria for Angelman syndrome; however, the nature and severity of anxiety symptoms have not been well characterised in this population. Anxiety behaviours, especially in response to separation from a preferred caregiver, have been described clinically but have not yet been explored empirically. METHOD: This study used a combination of standardised and clinician-derived survey items to assess the frequency, nature and severity of behaviours associated with anxiety and separation distress in 100 individuals with Angelman syndrome. Family (e.g. income and maternal education) and individual (e.g. age, sex, genetic subtype, sleep difficulties and aggressive behaviours) variables were also gathered to assess possible predictors of higher anxiety levels. Approximately half of the sample was seen in clinic and assessed with standardised measures of development and daily functioning, allowing for an additional exploration of the association between anxiety symptoms and extent of cognitive impairment. RESULTS: Anxiety concerns were reported in 40% of the sample, almost 70% were reported to have a preferred caregiver and over half displayed distress when separated from that caregiver. Individuals with the deletion subtype and individuals who are younger were less likely to have anxiety behaviours. Sleep difficulties and aggressive behaviour consistently significantly predicted total anxiety, the latter suggesting a need for future studies to tease apart differences between anxiety and aggression or anger in this population. CONCLUSIONS: Anxiety concerns, especially separation distress, are common in individuals with Angelman syndrome and represent an area of unmet need for this population.


Assuntos
Síndrome de Angelman/fisiopatologia , Ansiedade de Separação/fisiopatologia , Ansiedade/fisiopatologia , Cuidadores , Apego ao Objeto , Relações Pais-Filho , Pais , Angústia Psicológica , Adolescente , Adulto , Síndrome de Angelman/complicações , Síndrome de Angelman/epidemiologia , Ansiedade/epidemiologia , Ansiedade/etiologia , Ansiedade de Separação/epidemiologia , Ansiedade de Separação/etiologia , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Adulto Jovem
3.
J Intellect Disabil Res ; 62(10): 821-832, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-30105880

RESUMO

BACKGROUND: Little is known about how individuals with fragile X syndrome (FXS) and their families use technology in daily life and what skills individuals with FXS can perform when using mobile technologies. METHODS: Using a mixed-methods design, including an online survey of parents (n = 198) and a skills assessment of individuals with FXS (n = 6), we examined the experiences and abilities of individuals with FXS for engaging with mobile technology. RESULTS: Parents reported that individuals with FXS often used technology in their daily lives, with variations based on age of child, sex, autism status, depression, and overall ability. Parents frequently sought and shared FXS-related information online. Assessment data revealed that individuals with FXS demonstrated proficiency in interacting with technology. CONCLUSIONS: Mobile technology is a tool that can be used in FXS to build skills and increase independence rather than simply for recreational purposes. Implications for using mobile technology to enhance healthcare decision making are discussed.


Assuntos
Sistemas Computacionais , Síndrome do Cromossomo X Frágil , Deficiência Intelectual , Destreza Motora , Telecomunicações , Telemedicina , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Tomada de Decisão Clínica , Sistemas Computacionais/estatística & dados numéricos , Feminino , Síndrome do Cromossomo X Frágil/reabilitação , Humanos , Deficiência Intelectual/reabilitação , Internet/estatística & dados numéricos , Masculino , Pessoa de Meia-Idade , Pais , Inquéritos e Questionários , Telecomunicações/estatística & dados numéricos , Telemedicina/estatística & dados numéricos , Adulto Jovem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA