Tourette syndrome, obsessive compulsive behavior, and dysmorphic features in a patient with deletions at chromosome 18q22.1 and chromosome 13q12.3-q13.1

Parkinsonism Relat Disord. 2016 Nov:32:133-134. doi: 10.1016/j.parkreldis.2016.09.002. Epub 2016 Sep 4.
No abstract available

Keywords: 13q13 deletion; 18q22 deletion; Genetics; Tic disorder; Tics; Tourette syndrome.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Chromosome Deletion
  • Chromosome Disorders / genetics*
  • Chromosomes, Human, Pair 13 / genetics
  • Chromosomes, Human, Pair 18 / genetics
  • Craniofacial Abnormalities / genetics*
  • Humans
  • Male
  • Obsessive-Compulsive Disorder / genetics*
  • Tourette Syndrome / genetics*
  • Young Adult

Supplementary concepts

  • 13q deletion syndrome
  • Chromosome 18 deletion syndrome