9p monosomy in a patient with Gilles de la Tourette's syndrome

Lorna Taylor, David B. Krizman, Joseph Jankovic, A. Hayani, P Steuber, Frank Greenberg, Raymond G. Fenwick, C. Thomas Caskey

Neurology · 1991 · 50 citations · 0 references

Concepts

Abstract

Gilles de la Tourette's syndrome (GTS) is a genetic disorder characterized by multiple motor and vocal tics, obsessive-compulsive disorder, and attention-deficit disorder. Family studies support the presence of an autosomal dominant gene; however, to date, an assignment for the GTS locus has not been made. We present the case of a boy with GTS and a deletion of the terminal portion of the short arm of chromosome 9, del(9)(qter----p2304:).