Pilot Study of Familial Nonsyndromal Mondini Dysplasia

Purpose:

OBJECTIVES: I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.

Study summary:

PROTOCOL OUTLINE: 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.

Criteria:

PROTOCOL ENTRY CRITERIA: Parents of a study family with nonsyndromal Mondini dysplasia

NCT ID:

NCT00004336

Primary Contact:

Study Chair
Andrew J. Griffith
University of Michigan

Backup Contact:

N/A

Location Contact:

Ann Arbor, Michigan 48109
United States



There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: September 19, 2017

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