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3.
Neuroimage Clin ; 25: 102139, 2020.
Article in English | MEDLINE | ID: mdl-31887718

ABSTRACT

Down Syndrome (DS) is the most frequent genetic cause of intellectual disability with a wide spectrum of neurodevelopmental outcomes. At present, the relationship between structural brain morphology and the spectrum of cognitive phenotypes in DS, is not well understood. This study aimed to quantify the development of the fetal and neonatal brain in DS participants, with and without a congenital cardiac defect compared with a control population using dedicated, optimised and motion-corrected in vivo magnetic resonance imaging (MRI). We detected deviations in development and altered regional brain growth in the fetus with DS from 21 weeks' gestation, when compared to age-matched controls. Reduced cerebellar volume was apparent in the second trimester with significant alteration in cortical growth becoming evident during the third trimester. Developmental abnormalities in the cortex and cerebellum are likely substrates for later neurocognitive impairment, and ongoing studies will allow us to confirm the role of antenatal MRI as an early biomarker for subsequent cognitive ability in DS. In the era of rapidly developing technologies, we believe that the results of this study will assist counselling for prospective parents.


Subject(s)
Cerebellum , Cerebral Cortex , Down Syndrome/diagnostic imaging , Fetal Development , Fetus , Heart Defects, Congenital , Biomarkers , Cerebellum/abnormalities , Cerebellum/diagnostic imaging , Cerebellum/growth & development , Cerebral Cortex/abnormalities , Cerebral Cortex/diagnostic imaging , Cerebral Cortex/growth & development , Comorbidity , Down Syndrome/epidemiology , Down Syndrome/pathology , Female , Fetal Development/physiology , Fetus/abnormalities , Fetus/diagnostic imaging , Gestational Age , Heart Defects, Congenital/epidemiology , Humans , Infant, Newborn , Longitudinal Studies , Magnetic Resonance Imaging , Male , Pregnancy , Prenatal Diagnosis
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