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Home > "C" Clinical Trials Conditions > Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)

Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)



Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)

For Condition: Hereditary Ataxia
Status: Recruiting
Sponsor(s): National Institute of Neurological Disorders and Stroke (NINDS) , Baylor College of Medicine
Synopsis: OBJECTIVES: I. Clinically evaluate members from families with dominantly inherited ataxias and collect blood samples for detailed molecular studies. II. Perform detailed clinical evaluations on patients with recessively inherited ataxias.
Details: PROTOCOL OUTLINE: Participants undergo a comprehensive clinical and molecular evaluation. Studies include: neurologic evaluation, including magnetic resonance imaging and nerve conduction studies; ophthalmologic exam; audiologic exam, including auditory brain stem evoked response; DNA extraction for lymphoblastoid cell lines; gene mapping; and linkage analysis. A neuropathologic evaluation is conducted postmortem, when possible. Patients with recessive ataxia also receive a developmental assessment.
Eligibility:
Study Type:
  Observational, Screening
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: - Patients with recessive ataxia - Members of families with dominantly inherited ataxia
Total Enrollment: 30

Location and Contact Information:

Overall Study Official:
TetsuoAshizawa,  Study Chair,  Baylor College of Medicine

University of Texas Medical Branch at Galveston *Recruiting*
Galveston,  Texas,  77555
United States
Recruiting Tetsuo  Ashizawa 409-772-2466


Additional Information:
Study ID Numbers:
  199/11796;  BCM-H4499
Study Start Date: November 1999
Record last reviewed: October 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00004306

Other Hereditary Ataxia Studies:
1. Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)

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