| Literature DB >> 32507511 |
Ilaria Parenti1, Luis G Rabaneda1, Hanna Schoen1, Gaia Novarino2.
Abstract
Neurodevelopmental disorders (NDDs) are a class of disorders affecting brain development and function and are characterized by wide genetic and clinical variability. In this review, we discuss the multiple factors that influence the clinical presentation of NDDs, with particular attention to gene vulnerability, mutational load, and the two-hit model. Despite the complex architecture of mutational events associated with NDDs, the various proteins involved appear to converge on common pathways, such as synaptic plasticity/function, chromatin remodelers and the mammalian target of rapamycin (mTOR) pathway. A thorough understanding of the mechanisms behind these pathways will hopefully lead to the identification of candidates that could be targeted for treatment approaches.Entities:
Keywords: gene vulnerability; molecular pathways; mutational load; neurodevelopmental disorders; next-generation sequencing
Year: 2020 PMID: 32507511 DOI: 10.1016/j.tins.2020.05.004
Source DB: PubMed Journal: Trends Neurosci ISSN: 0166-2236 Impact factor: 13.837