Charting the future: current and future directions in translational research for individuals with Down syndrome

Abstract The most common genetic cause of intellectual and developmental disability is trisomy of human chromosome 21 (trisomy 21) or Down syndrome. Relative to the general population, individuals with Down syndrome heterogeneously experience atypical morphogenesis, a distinct neurocognitive profile...

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Autori principali:	Katherine A. Waugh, Heather M. Wilkins, Keith P. Smith, Lauren T. Ptomey
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMC 2025-07-01
Serie:	Journal of Neurodevelopmental Disorders
Soggetti:	Down syndrome Trisomy 21 Intellectual and Developmental Disability Precision Medicine Brain Health Biomarkers
Accesso online:	https://doi.org/10.1186/s11689-025-09630-8
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