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Altered Brain Structure in Infants with Turner Syndrome.
Davenport, M L; Cornea, E; Xia, K; Crowley, J J; Halvorsen, M W; Goldman, B D; Reinhartsen, D; DeRamus, M; Pretzel, R; Styner, M; Gilmore, J H; Hooper, S R; Knickmeyer, R C.
Afiliação
  • Davenport ML; Department of Pediatrics, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Cornea E; Department of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Xia K; Department of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Crowley JJ; Department of Genetics, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Halvorsen MW; Department of Genetics, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Goldman BD; Frank Porter Graham Child Development Institute, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Reinhartsen D; Department of Psychology & Neuroscience, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • DeRamus M; Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Pretzel R; Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Styner M; Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Gilmore JH; Department of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Hooper SR; Department of Computer Science, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
  • Knickmeyer RC; Department of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
Cereb Cortex ; 30(2): 587-596, 2020 03 21.
Article em En | MEDLINE | ID: mdl-31216015
ABSTRACT
Turner syndrome (TS) is a genetic disorder affecting approximately 12000 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Turner / Encéfalo Limite: Female / Humans / Infant Idioma: En Revista: Cereb Cortex Assunto da revista: CEREBRO Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Turner / Encéfalo Limite: Female / Humans / Infant Idioma: En Revista: Cereb Cortex Assunto da revista: CEREBRO Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos