Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2 participants
OBSERVATIONAL
1995-10-31
Brief Summary
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I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.
Detailed Description
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The parents of 1 family with known Mondini dysplasia are screened for the disorder using temporal bone computerized tomography without contrast. This information is used to determine the mode of inheritance.
Conditions
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Eligibility Criteria
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Inclusion Criteria
Parents of a study family with nonsyndromal Mondini dysplasia
0 Years
ALL
No
Sponsors
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University of Michigan
OTHER
National Center for Research Resources (NCRR)
NIH
Principal Investigators
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Andrew J. Griffith
Role: STUDY_CHAIR
University of Michigan
Locations
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University of Michigan Health Systems
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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UMMC-1402
Identifier Type: -
Identifier Source: secondary_id
199/11895
Identifier Type: -
Identifier Source: org_study_id