Sengun, EceYararbas, KanayKasakyan, SerdarAlanay, Yasemin2024-07-122024-07-1220161552-48251552-483310.1002/ajmg.a.378822-s2.0-84995780916https://dx.doi.org/10.1002/ajmg.a.37882https://hdl.handle.net/20.500.12415/7736Here we summarize the clinical and molecular findings in a 68-year-old female with dysmorphic features, mild-to-moderate intellectual disability, and behavioral findings suggesting autism spectrum disorder. SNP array analysis demonstrated a 257 kb deletion comprising exon 6 of AUTS2. This clinical report provides the natural history in the eldest patient yet to be reported, and complements the existing evidence suggesting that disruption of the AUTS2 leads to a recently delineated neurodevelopmental phenotype with a wide spectrum, namely "AUTS2 Syndrome." (C) 2016 Wiley Periodicals, Inc.eninfo:eu-repo/semantics/closedAccessAUTS2intellectual disabilityautism spectrum disorderdevelopmental delayArticle32361227531620Q23231170WOS:000388199100026Q3