Pilot Study of Familial Nonsyndromal Mondini Dysplasia

N

National Center for Research Resources (NCRR)

Status

Completed

Conditions

Mondini Dysplasia

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT00004336
UMMC-1402
199/11895

Details and patient eligibility

About

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

Full description

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.

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

PROTOCOL ENTRY CRITERIA:

Parents of a study family with nonsyndromal Mondini dysplasia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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