| Literature DB >> 26468184 |
Renata Bartesaghi1, Tarik F Haydar2, Jean Maurice Delabar3, Mara Dierssen4, Carmen Martínez-Cué5, Diana W Bianchi6.
Abstract
Down syndrome (DS) is a relatively common genetic condition caused by the triplication of human chromosome 21. No therapies currently exist for the rescue of neurocognitive impairment in DS. This review presents exciting findings showing that it is possible to restore brain development and cognitive performance in mouse models of DS with therapies that can also apply to humans. This knowledge provides a potential breakthrough for the prevention of intellectual disability in DS.Entities:
Keywords: Down syndrome; brain abnormalities; intellectual disability; mouse models; preventive therapies
Mesh:
Year: 2015 PMID: 26468184 PMCID: PMC6608177 DOI: 10.1523/JNEUROSCI.2775-15.2015
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167