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.
|United States, Michigan|
|University of Michigan Health Systems|
|Ann Arbor, Michigan, United States, 48109|
|Study Chair:||Andrew J. Griffith||University of Michigan|