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Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases



Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases

For Condition: Movement Disorders,Myoclonus,Nervous System Diseases,Tic Disorders,Tremor
Status: Completed
Sponsor(s): National Institute of Neurological Disorders and Stroke (NINDS) ,
Synopsis: 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.
Details: 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.
Eligibility:
Study Type:
  Observational, Natural History
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: Neurologic disease or movement disorders affecting 2 or more family members. No conditions in which phlebotomy is contra-indicated.
Total Enrollment: 300

Location and Contact Information:

National Institute of Neurological Disorders and Stroke (NINDS)
Bethesda,  Maryland,  20892
United States
 


Additional Information:
Study ID Numbers:
  970097;  97-N-0097
Study Start Date: March 26, 1997
Record last reviewed: February 18, 1999
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00001667

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1. Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases

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