Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00001667

Enrollment

300

Registered

2002-12-10

Start date

1997-03-31

Completion date

2000-04-30

Last updated

2008-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Movement Disorders, Myoclonus, Nervous System Diseases, Tic Disorders, Tremor

Keywords

Family Studies, Genetic, Myoclonus, Tics, Tremor, Movement Disorders, Neurological Disease

Brief summary

The purpose of this protocol is to identify families with inherited neurologic conditions, especially movement disorders, to evaluate affected and unaffected individuals clinically, and to obtain blood samples for genetic analysis.

Detailed description

Interventions

None listed

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

Neurologic disease or movement disorders affecting 2 or more family members. No conditions in which phlebotomy is contra-indicated.

Countries

United States

Outcome results