“…DS is the most common genetic cause of intellectual disability (ID) and impacts approximately 1 in 700 live births ( Mai et al, 2019 ). ID in DS manifests as impairments in language acquisition, executive functioning (i.e., attention, self-control, future planning), and hippocampal-dependent declarative memory ( Carlesimo et al, 1997 ; Vicari et al, 2000 ; Nadel, 2003 ; Cornish et al, 2007 ; Trezise et al, 2008 ; Lanfranchi et al, 2010 ; Costanzo et al, 2013 ; Godfrey and Lee, 2018 ; Dimachkie Nunnally et al, 2023 ), ranging from moderate to severe with intelligent quotient (IQ) scores between 30 and 70 ( Gueant et al, 2005 ; Määttä et al, 2006 ). Individuals with DS are at a greater risk of neurological comorbidities such as epilepsy ( Goldberg-Stern et al, 2001 ; Altuna et al, 2021 ), Alzheimer’s disease ( Mann, 1988 ; McCarron et al, 2017 ; Snyder et al, 2020 ), and attention deficit hyperactivity disorder (ADHD) ( Capone et al, 2006 ).…”