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    AUTS2 Syndrome in a 68-Year-Old Female: Natural History and Further Delineation of the Phenotype
    (WILEY-BLACKWELL, 2016) Sengun, Ece; Yararbas, Kanay; Kasakyan, Serdar; Alanay, Yasemin
    Here 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.