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133900 https://hdl.handle.net/2286/R.I.47766 http://rightsstatements.org/vocab/InC/1.0/ 2018-05 18 pages eng Philp, Jennifer Lynn Scherer, Nancy Peter, Beate Department of Speech and Hearing Science Sanford School of Social and Family Dynamics Barrett, The Honors College Text 22q11.2 Deletion Syndrome (22q11.2DS) is one of the most frequent chromosomal microdeletion syndromes in humans. This case study focuses on the language and reading profile of a female adult with 22q11.2 Deletion Syndrome who was undiagnosed until the age of 27 years old. To comprehensively describe the participant's profile, a series of assessment measures was administered in the speech, language, cognition, reading, and motor domains. Understanding how 22q11.2DS has impacted the life of a recently diagnosed adult will provide insight into how to best facilitate long-term language and educational support for this population and inform future research. Speech and Hearing Science Genetics 22q11.2 Deletion Syndrome The Adult Communication, Cognitive, and Reading Profile of 22q11.2 Deletion Syndrome