Examination of the SGCE gene in Tourette's syndrome patients with obsessive-compulsive disorder

Patricia de Carvalho Aguiar, Melissa Fazzari, Joseph Jankovic, Laurie J. Ozelius

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Mutations in the ε-sarcoglycan gene (SGCE) have been reported in families with myoclonus-dystonia (M-D). In addition to abnormal movements, obsessive-compulsive disorder (OCD) has also been described in families with M-D. OCD is a common feature in another movement disorder, namely Tourette's syndrome (TS). The comorbidity of these disorders suggests that common genetic factors might be involved in their susceptibility. To evaluate this, we performed two sets of experiments. An association study using a polymorphism within an intron of the SGCE gene was assessed in patients with TS and OCD versus controls, and the SGCE gene itself was screened for mutations in all TS/OCD patients, followed by direct sequencing of the gene in a limited number of these patients. No correlation was found by either method.

Original languageEnglish (US)
Pages (from-to)1237-1238
Number of pages2
JournalMovement Disorders
Volume19
Issue number10
DOIs
StatePublished - Oct 1 2004

Fingerprint

Sarcoglycans
Tourette Syndrome
Obsessive-Compulsive Disorder
Genes
Mutation
Dyskinesias
Movement Disorders
Introns
Comorbidity

Keywords

  • ε-sarcoglycan
  • Myoclonus-dystonia
  • Obsessive-compulsive disorder
  • Tourette's syndrome

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Examination of the SGCE gene in Tourette's syndrome patients with obsessive-compulsive disorder. / de Carvalho Aguiar, Patricia; Fazzari, Melissa; Jankovic, Joseph; Ozelius, Laurie J.

In: Movement Disorders, Vol. 19, No. 10, 01.10.2004, p. 1237-1238.

Research output: Contribution to journalArticle

de Carvalho Aguiar, Patricia ; Fazzari, Melissa ; Jankovic, Joseph ; Ozelius, Laurie J. / Examination of the SGCE gene in Tourette's syndrome patients with obsessive-compulsive disorder. In: Movement Disorders. 2004 ; Vol. 19, No. 10. pp. 1237-1238.
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