Pilot Study of Familial Nonsyndromal Mondini Dysplasia
I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.
|Study Design:||Primary Purpose: Screening|
|Study Start Date:||October 1995|
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.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00004336
|United States, Michigan|
|University of Michigan Health Systems|
|Ann Arbor, Michigan, United States, 48109|
|Study Chair:||Andrew J. Griffith||University of Michigan|