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Pilot Study of Familial Nonsyndromal Mondini Dysplasia

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ClinicalTrials.gov Identifier: NCT00004336
Recruitment Status : Completed
First Posted : October 19, 1999
Last Update Posted : June 24, 2005
Sponsor:
Collaborator:
University of Michigan
Information provided by:
National Center for Research Resources (NCRR)

Brief Summary:

OBJECTIVES:

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


Condition or disease
Mondini Dysplasia

Detailed 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.


Study Type : Observational
Enrollment : 2 participants
Primary Purpose: Screening
Study Start Date : October 1995

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U.S. FDA Resources





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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

PROTOCOL ENTRY CRITERIA:

Parents of a study family with nonsyndromal Mondini dysplasia


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00004336


Locations
United States, Michigan
University of Michigan Health Systems
Ann Arbor, Michigan, United States, 48109
Sponsors and Collaborators
National Center for Research Resources (NCRR)
University of Michigan
Investigators
Study Chair: Andrew J. Griffith University of Michigan

ClinicalTrials.gov Identifier: NCT00004336     History of Changes
Other Study ID Numbers: 199/11895
UMMC-1402
First Posted: October 19, 1999    Key Record Dates
Last Update Posted: June 24, 2005
Last Verified: April 2002

Keywords provided by National Center for Research Resources (NCRR):
Mondini dysplasia
genetic diseases and dysmorphic syndromes
rare disease