5 CASES DEMONSTRATING THE DISTINCTIVE BEHAVIORAL FEATURES OF CHROMOSOME DELETION 17(P11.2 P11.2) (SMITH-MAGENIS SYNDROME)

Abstract Children with hyperactivity and self‐destructive behaviour present a difficult problem for parents and paediatricians. The syndrome described by Smith and Magenis is due to a deletion on the short arm of chromosome 17: del(17)(p 11.2 p 11.2). Clinical manifestations include brachycephaly and a flat mid‐face; brachydactyly; short, broad hands; mental retardation; and aberrant behaviour, including hyperactivity. We report on five children, and review the literature on a newly recognised syndrome in which the behaviour manifestations may precede and often overshadow the learning disabilities and unusual appearance. In addition, we have found sleep disturbance to be a major feature in our patients. Copyright © 1990, Wiley Blackwell. All rights reserved