17,18 Several biological pathways identified Individuals with ASD vary in language ability, ranging from absent speech to fluent language, and in cognitive development, ranging from profound intellectual disability to above-average intellectual functioning. Individuals may also show associated medical comorbidities including epilepsy and minor physical anomalies, as well as psychiatric comorbidities,

thus showing a wide clinical heterogeneity. The clinical heterogeneity Inhibitors,research,lifescience,medical of autism has long been a hindrance to understanding the pathophysiological mechanisms involved. However, although many questions remain and new questions are

Inhibitors,research,lifescience,medical being raised, the last several years of investigation have brought important pieces to the autism puzzle. Indeed, the identification of specific alleles contributing to ASD has shed light on pathogenic mechanisms. The only consensus regarding the mode of inheritance Inhibitors,research,lifescience,medical of autism is that it is not Mendelian, at least in a vast majority of cases. Several studies were initially in favor of a polygenic model.19-21 Therefore, the initial strategy to unravel genetic factors increasing autism risk was to build large cohorts for linkage and association studies. Given the lack of replication of the results, consortia gathering several cohorts were created to increase the power of the studies, Inhibitors,research,lifescience,medical but without clear results. With regard to nonparametric linkage, the largest study to date included 1181 multiplex families22 and did not identify highly

significant evidence for linkage. Moreover, the three large studies using genome -wide association that have been published thus far each highlight a single, non-overlapping risk locus.23-25 These findings led some Inhibitors,research,lifescience,medical authors to predict that few, if any, common variants have a substantial impact on risk (odds ratio >1.2), but many common variants could have a more modest impact.26 Going back to an individual approach, already used in mental retardation, the search for Dichloromethane dehalogenase rare mutations or chromosomal rearrangements was then used, allowing new hypotheses about the mechanisms involved in autism. While the existence of many genetic check details syndromes associated with autism first led to considering the existence of genetic heterogeneity mirroring the clinical variability, genetic studies in idiopathic autism confirmed the existence of different defects in common pathways. The results suggest that autism may be caused by a multitude of genetic alterations that ultimately affect only limited biological pathways of brain development and plasticity.