Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT00018889

Phenotype/Genotype Correlations in Movement Disorders

Sponsor: National Institute of Neurological Disorders and Stroke (NINDS)

View on ClinicalTrials.gov

Summary

The goal of this protocol is to identify families with inherited movement disorders and evaluate disease manifestations to establish an accurate clinical diagnosis by using newest technological advances and investigate the underlying molecular mechanisms. Studies of inherited movement disorders in large families with good genealogical records are especially valuable. Patients with diseases of known molecular basis will be genotyped in order to investigate phenotype/genotype correlation. Patients with disease of unknown or incomplete genetic characterization will be studied with a hope of contributing to the identification of specific disease-causing genes and genetic mechanisms responsible for a specific disorder.

Key Details

Gender

All

Age Range

2 Years - 100 Years

Study Type

OBSERVATIONAL

Enrollment

2500

Start Date

2001-10-22

Completion Date

Not specified

Last Updated

2026-03-25

Healthy Volunteers

No

Locations (1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States