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| ID | Type | Description | Link |
|---|---|---|---|
| UMMC-1402 |
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| Name | Class |
|---|---|
| University of Michigan | OTHER |
OBJECTIVES:
I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.
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.
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PROTOCOL ENTRY CRITERIA:
Parents of a study family with nonsyndromal Mondini dysplasia
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| Name | Affiliation | Role |
|---|---|---|
| Andrew J. Griffith | University of Michigan | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Michigan Health Systems | Ann Arbor | Michigan | 48109 | United States |
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| ID | Term |
|---|---|
| D030342 | Genetic Diseases, Inborn |
| D035583 | Rare Diseases |
| ID | Term |
|---|---|
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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