Autism with known genetic associations: implications for ‘idiopathic’ autism

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Caitlin Clements, Tara L. Wenger, Judi Miller, Ashley de Marchena, Alisa Zoltowski, Lauren DePolo, D. M. McDonald-McGinn, E. H. Zackai, B. Emanuel, Robert T. Schultz

Abstract Text: 

Genetic syndromes associated with autism spectrum disorder (ASD) have been studied intensely in the hope of understanding the biology of these disorders and of ASD in general.  These ASDs associated with mutations have become an important part of a genotype-first strategy for parsing the heterogeneity of ASD, illuminating the pathophysiology, and defining targets for pharmacological treatment. Prime examples include research on Fragile X and copy number variants such as 16p11.2 and 22q11.2. However, it remains unknown how well treatments based on these genetically defined forms of ASD will generalize to ‘idiopathic’ ASD. This uncertainty stems from the genomic heterogeneity of ASD and from the phenotypic heterogeneity within each syndrome. This panel examines four examples of this genotype-first strategy: Fragile X, 22q11.2 copy number variants, and disruptions in SCN2A and DYRK1A. Discussion will focus on phenotypic heterogeneity, implications for translational research, and the challenges to assessing clinical outcomes. Presentations will include an analysis of familial phenotypes (DYRK1A), identification of a critical region for ASD risk in 22q11.2, genotype-phenotype correlations observed in SCN2A mutations, and differences in language and social communication trajectories between idiopathic ASD and Fragile X syndrome.

 

 

Talks

1. Title: Opposing effects on NaV1.2 function underlie differences between SCN2A variants observed in individuals with autism spectrum disorder or infantile seizures

Authors: Roy Ben-Shalom, Caroline M. Keeshen, Kiara N. Berrios, Joon Y. An, Kevin J. Bender, and Stephan J. Sanders

 

2. Title: Phenotypic characterization and identification of a critical region associated with autism in individuals with deletions and duplications of 22q11.2

Authors: Caitlin Clements, Tara L. Wenger, Judi Miller, Ashley de Marchena, Alisa Zoltowski, Lauren DePolo, D. M. McDonald-McGinn, E. H. Zackai, B. Emanuel, Robert T. Schultz

 

3. Title: Phenotypic presentation and the role of parental phenotype in accounting for variability in individuals with disruptive DYRK1A mutations

Authors: Earl, R.K., Hudac, C.M., Gerdts, J., & Bernier, R.

 

4. Title: Understanding the Comorbidity of Autism Spectrum Disorder and Fragile X Syndrome: Moving Beyond a Categorical Approach

Authors: Leonard Abbeduto, Angela John Thurman, and Andrea McDuffie

 

Presentation Date and Time: 
Friday, May 12, 2017 - 10:00am