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Hypogyrification and its association with cognitive impairment in children with 22q11.2 deletion Syndrome: A preliminary report.
Lutz, Olivia; Lizano, Paulo; Mothi, Suraj Sarvode; Joseph, Adam; Tandon, Neeraj; Ormston, Leighanne; Hooper, Stephen; Keshavan, Matcheri; Shashi, Vandana.
Afiliação
  • Lutz O; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA. Electronic address: olutz@bidmc.harvard.edu.
  • Lizano P; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
  • Mothi SS; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA.
  • Joseph A; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA.
  • Tandon N; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA.
  • Ormston L; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA.
  • Hooper S; Department of Allied Health Sciences, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
  • Keshavan M; Department of Psychiatry, Beth Israel Deaconess Medical Center, 75 Fenwood Road, Room 551, Boston, MA, 02115, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
  • Shashi V; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
Psychiatry Res Neuroimaging ; 285: 47-50, 2019 03 30.
Article em En | MEDLINE | ID: mdl-30743074
ABSTRACT
22q11.2 Deletion Syndrome (22qDS) is a neurogenetic disorder resulting in cognitive deficits and hypogyrification, but relationships between these processes have not been established. 22qDS youth and healthy controls (HC) were administered a battery of cognitive tasks. Gyrification measurements were extracted from structural T1 scans using Freesurfer, contrasted between groups, and correlated to cognition. Data was adjusted for age, sex, socio-economic status and intracranial volume. 22qDS displayed significant hypogyrification which was associated with poorer executive functioning and verbal learning in orbitofrontal and anterior cingulate cortex. Our preliminary findings identified neurodevelopmental deficits in 22qDS shown by hypogyria, which relate to cognitive impairments.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Disfunção Cognitiva Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Psychiatry Res Neuroimaging Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Disfunção Cognitiva Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Psychiatry Res Neuroimaging Ano de publicação: 2019 Tipo de documento: Article