SA15 THE EMORY 3Q29 DELETION PROJECT: PROFILES OF NEURODEVELOPMENTAL AND NEUROPSYCHIATRIC PHENOTYPES
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DOI: 10.1016/j.euroneuro.2017.08.087
Abstract: Background 3q29 Deletion Syndrome (3q29DS) is a rare (~1:30000) genomic disorder characterized by a 1.6 Mb deletion on chromosome 3, and is associated with developmental delay, intellectual disability, and a significantly increased risk for neuropsychiatric disorders,… read more here.
Keywords: prevalence asd; diagnosis asd; 3q29 deletion; deletion ... See more keywords
G493 Adverse childhood experiences (ACE) and other correlates in children presenting for autism spectrum disorder(ASD) diagnosis
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DOI: 10.1136/archdischild-2017-313087.485
Abstract: Aims To determine whether adverse childhood experiences (ACE) influence child behaviour and correlation with final diagnosis of ASD in a cohort of children referred for a diagnosis of autism spectrum disorder (ASD). Methods We did… read more here.
Keywords: diagnosis asd; diagnosis; childhood; child ... See more keywords
Diagnosis-Based Hybridization of Multimedical Tests and Sociodemographic Characteristics of Autism Spectrum Disorder Using Artificial Intelligence and Machine Learning Techniques: A Systematic Review
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DOI: 10.1155/2022/3551528
Abstract: Autism spectrum disorder (ASD) is a complex neurobehavioral condition that begins in childhood and continues throughout life, affecting communication and verbal and behavioral skills. It is challenging to discover autism in the early stages of… read more here.
Keywords: spectrum disorder; diagnosis; diagnosis asd; autism spectrum ... See more keywords