Childhood Onset Dystonia, Chorea or Related Movement Disorder Panel

Overview

Test Name

Childhood Onset Dystonia, Chorea or Related Movement Disorder Panel

Test Code

NUE1015

Test Category

Gene Panels

Test Subcategory

Neurology

Disease(s) Targeted

Childhood Onset Dystonia, Chorea or Related Movement Disorder

Who Is The Test For?

Patients with a family history, clinical suspicion, or diagnosis of dystonia, chorea or related movement disorder with onset in childhood.

Test Approach

Whole exome sequencing (WES) with in silico gene panel analysis.

No. of Genes

190

Panel Content

Download Panel Content

Deliverables

Clinical Report (Download a sample report here)

Turnaround Time

~3-6 weeks*

Specimen Requirements

For detailed information about the sample requirements, please consult our clinical sample requirements page.

*Turnaround times are estimated from receipt of satisfactory specimen and test request form at the laboratory to release of clinical report. The turnaround time may vary depending on the nature of the specimen and the complexity of the investigation required. The above table is only a guideline and the complexity of a case and the requirement for further investigations may change this.

About Childhood Onset Dystonia, Chorea or Related Movement Disorder

Childhood onset dystonia, chorea, and related movement disorders involve involuntary muscle contractions and movements that begin in childhood or adolescence. These conditions can affect coordination and quality of life, making early diagnosis and treatment essential.