Response to name and its value for the early detection of developmental disorders: Insights from autism spectrum disorder, Rett syndrome, and fragile X syndrome. A perspectives paper
| Autor: | Katrin D. Bartl-Pokorny, Christa Einspieler, Laurie McLay, Jeff Sigafoos, Peter B. Marschik, Dajie Zhang, Magdalena Krieber, Sven Bölte, Luise Poustka, Laura Roche, Markus Gugatschka |
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| Rok vydání: | 2018 |
| Předmět: |
Autism Spectrum Disorder
Developmental Disabilities Prefrontal Cortex Early detection Rett syndrome Behavioral Symptoms Article 03 medical and health sciences Typically developing 0302 clinical medicine 030225 pediatrics Reaction Time Rett Syndrome Developmental and Educational Psychology medicine Humans Names Interpersonal Relations 0501 psychology and cognitive sciences Spectroscopy Near-Infrared 05 social sciences Infant medicine.disease Developmental disorder Fragile X syndrome Clinical Psychology Early Diagnosis Autism spectrum disorder Fragile X Syndrome Psychology 050104 developmental & child psychology Clinical psychology |
| Zdroj: | Research in Developmental Disabilities. 82:95-108 |
| ISSN: | 0891-4222 |
| DOI: | 10.1016/j.ridd.2018.04.004 |
| Popis: | Background Responding to one’s own name (RtN) has been reported as atypical in children with developmental disorders, yet comparative studies on RtN across syndromes are rare. Aims We aim to (a) overview the literature on RtN in different developmental disorders during the first 24 months of life, and (b) report comparative data on RtN across syndromes. Methods and procedures In Part 1, a literature search, focusing on RtN in children during the first 24 months of life with developmental disorders, identified 23 relevant studies. In Part 2, RtN was assessed utilizing retrospective video analysis for infants later diagnosed with ASD, RTT, or FXS, and typically developing peers. Outcomes and results Given a variety of methodologies and instruments applied to assess RtN, 21/23 studies identified RtN as atypical in infants with a developmental disorder. We observed four different developmental trajectories of RtN in ASD, RTT, PSV, and FXS from 9 to 24 months of age. Between-group differences became more distinctive with age. Conclusions and implications RtN may be a potential parameter of interest in a comprehensive early detection model characterising age-specific neurofunctional biomarkers associated with specific disorders, and contribute to early identification. |
| Databáze: | OpenAIRE |
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