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Using the Visual World Paradigm to Study Sentence Comprehension in Mandarin-Speaking Children with Autism
Published on: October 3, 2018
Autism or autisms? Finding the lowest common denominator
Emily L Williams1, Manuel F Casanova
1Department of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, Kentucky 40202, USA.
Abstract:
Previous studies suggest the presence of a minicolumnopathy in autism. Minicolumnar abnormalities as well as certain migratory and proliferative defects, common to autism, may be rooted in the general mechanics of periventricular germinal cell division and maturation. Increased numbers of periventricular germinal cell/radial glia can be mimicked by a variety of different transgenic mouse models and environmental factors. These murine models and environmental factors illustrate how a fairly homogenous neuroanatomical phenotype can diverge at the genetic level. By first defining the lowest common denominator (i.e., the minicolumn) and then examining which pathways are vulnerable to involved genetic and environmental factors, we may gain a greater understanding of the pathophysiologic mechanisms underlying Autism Spectrum Conditions.
Insights
Autism Spectrum Conditions may involve minicolumnopathy, a brain structure abnormality. Understanding periventricular germinal cell defects in mouse models offers insights into autism
Area of Science:
- Neuroscience
- Developmental Biology
- Genetics
Background:
- Autism Spectrum Conditions (ASC) are increasingly linked to neuroanatomical abnormalities.
- Previous research suggests a potential 'minicolumnopathy' in individuals with autism.
- Cellular defects in migration and proliferation are common in ASC.
Purpose of the Study:
- To explore the potential link between periventricular germinal cell division and maturation defects and minicolumnar abnormalities in autism.
- To investigate how genetic and environmental factors contribute to these neurodevelopmental alterations.
- To identify common pathways underlying ASC pathophysiology.
Main Methods:
- Review of existing literature on minicolumnar structure in autism.
- Analysis of transgenic mouse models exhibiting periventricular germinal cell/radial glia increases.
- Examination of environmental factors implicated in autism neurodevelopment.
- Comparative analysis of genetic versus environmental influences on neuroanatomical phenotypes.
Main Results:
- Increased numbers of periventricular germinal cells/radial glia are observed in various autism models.
- These cellular changes can be induced by both genetic modifications and environmental exposures.
- A homogenous neuroanatomical phenotype (minicolumnopathy) can arise from diverse genetic underpinnings.
Conclusions:
- Minicolumnar abnormalities in autism may stem from disruptions in early cell division and maturation processes.
- Studying the minicolumn as a fundamental unit can help elucidate the diverse genetic and environmental pathways contributing to ASC.
- This approach may reveal common pathophysiologic mechanisms across different autism etiologies.
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