Pilot Study of Familial Nonsyndromal Mondini Dysplasia
NCT00004336 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2
Last updated 2005-06-24
Summary
OBJECTIVES:
I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.
Conditions
- Mondini Dysplasia
Sponsors & Collaborators
- collaborator OTHER
-
National Center for Research Resources (NCRR)
lead NIH
Principal Investigators
-
Andrew J. Griffith · University of Michigan
Eligibility
- Min Age
- 0 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1995-10-31
Countries
- United States
Study Locations
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