Fragile X syndrome (FXS) is the leading known inherited cause of intellectual disability and the most common known biological cause of autism. Approximately 25% to 50% of males with FXS meet full diagnostic criteria for autism. Despite the high comorbidity between FXS and autism and the ability to diagnose FXS prenatally or at birth, no studies have examined indicators of autism in infants with FXS. The current study focused on indices of visual attention, one of the earliest and most robust behavioral indicators of autism in idiopathic (non-FXS) autism. Analyses revealed lower HR variability, shallower HR decelerations, and prolonged look durations in 12-month old infants with FXS that were correlated with severity of autistic behavior but...
Prior research suggests that 60–74% of males and 16–45% of females with fragile X syndrome (FXS) mee...
Basic attentional processes and their impact on developmental trajectories in fragile X syndrome wer...
Autism is an etiologically heterogeneous neurodevelopmental disorder for which there is no known uni...
Fragile X syndrome (FXS) is the leading known inherited cause of intellectual disability and the mos...
Fragile X syndrome (FXS) is the leading known inherited cause of intellectual disability and the mos...
Fragile X syndrome (FXS) is the leading known genetic cause of autism spectrum disorder (ASD) with 6...
One of the major difficulties concerning Fragile X Syndrome has been early diagnosis enabling early ...
Objective To describe the development of young boys with fragile X syndrome (FXS). Methods Fifty-fiv...
AbstractStudies have reported that a selective deficit in visual motion processing is present in cer...
Characterizing early predictors of autism facilitates earlier identification, diagnosis and treatmen...
Background: Fragile X syndrome (FXS) is an early diagnosed monogenic disorder, associated with a st...
IMPORTANCE Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder and the most common inh...
To examine patterns of early brain growth in young children with fragile X syndrome (FXS) compared t...
Previous research of the behavioral phenotype in fragile X syndrome (FXS) has found that boys with F...
This study characterized the rates of rates of attention-deficit/hyperactivity disorder (ADHD) in ad...
Prior research suggests that 60–74% of males and 16–45% of females with fragile X syndrome (FXS) mee...
Basic attentional processes and their impact on developmental trajectories in fragile X syndrome wer...
Autism is an etiologically heterogeneous neurodevelopmental disorder for which there is no known uni...
Fragile X syndrome (FXS) is the leading known inherited cause of intellectual disability and the mos...
Fragile X syndrome (FXS) is the leading known inherited cause of intellectual disability and the mos...
Fragile X syndrome (FXS) is the leading known genetic cause of autism spectrum disorder (ASD) with 6...
One of the major difficulties concerning Fragile X Syndrome has been early diagnosis enabling early ...
Objective To describe the development of young boys with fragile X syndrome (FXS). Methods Fifty-fiv...
AbstractStudies have reported that a selective deficit in visual motion processing is present in cer...
Characterizing early predictors of autism facilitates earlier identification, diagnosis and treatmen...
Background: Fragile X syndrome (FXS) is an early diagnosed monogenic disorder, associated with a st...
IMPORTANCE Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder and the most common inh...
To examine patterns of early brain growth in young children with fragile X syndrome (FXS) compared t...
Previous research of the behavioral phenotype in fragile X syndrome (FXS) has found that boys with F...
This study characterized the rates of rates of attention-deficit/hyperactivity disorder (ADHD) in ad...
Prior research suggests that 60–74% of males and 16–45% of females with fragile X syndrome (FXS) mee...
Basic attentional processes and their impact on developmental trajectories in fragile X syndrome wer...
Autism is an etiologically heterogeneous neurodevelopmental disorder for which there is no known uni...