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Direct linkJiménez-Romero, Ma Salud; Fernández-Urquiza, Maite; Benítez-Burraco, Antonio – Journal of Speech, Language, and Hearing Research, 2022
Purpose: Chromosome 16p11.2 deletion syndrome (OMIM #611913) is a rare genetic condition resulting from the partial deletion of approximately 35 genes located at Chromosome 16. Affected people exhibit a variable clinical profile, featuring mild dysmorphisms, motor problems, developmental delay, mild intellectual disability (ID), socialization…
Descriptors: Genetic Disorders, Disabilities, Language Impairments, Communication Disorders
McLeod, Sharynne; McKinnon, David H. – International Journal of Language & Communication Disorders, 2007
Background: Prevalence data are of interest to health professionals and educators to assist in the planning of service delivery, allow for the calculation of the level of impact of intervention, and allow for the consideration of the boundaries between typical development and impairment. Aims: To determine the prevalence of children with…
Descriptors: Secondary School Students, Learning Problems, Incidence, Visual Impairments
Haslam, Robert H. A., Ed.; Valletutti, Peter J., Ed. – 1996
Intended for educators needing information on common medical disorders in the school setting, this book stresses the role of the teacher in referral and diagnosis and offers 22 chapters by experts in their various fields. Chapter titles and authors are: (1) "The Crucial Role of the Teacher" (Peter J. Valletutti); (2) "Prevention of…
Descriptors: Adolescents, Attention Deficit Disorders, Behavior Disorders, Cerebral Palsy
