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Pilot Study of Familial Nonsyndromal Mondini Dysplasia

This study has been completed.
University of Michigan
Information provided by:
National Center for Research Resources (NCRR) Identifier:
First received: October 18, 1999
Last updated: June 23, 2005
Last verified: April 2002


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

Mondini Dysplasia

Study Type: Observational
Study Design: Primary Purpose: Screening

Resource links provided by NLM:

Further study details as provided by National Center for Research Resources (NCRR):

Estimated Enrollment: 2
Study Start Date: October 1995
Detailed Description:


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.


Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No


Parents of a study family with nonsyndromal Mondini dysplasia

  Contacts and Locations
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Please refer to this study by its identifier: NCT00004336

United States, Michigan
University of Michigan Health Systems
Ann Arbor, Michigan, United States, 48109
Sponsors and Collaborators
University of Michigan
Study Chair: Andrew J. Griffith University of Michigan
  More Information

No publications provided Identifier: NCT00004336     History of Changes
Other Study ID Numbers: 199/11895, UMMC-1402
Study First Received: October 18, 1999
Last Updated: June 23, 2005
Health Authority: United States: Federal Government

Keywords provided by National Center for Research Resources (NCRR):
Mondini dysplasia
genetic diseases and dysmorphic syndromes
rare disease processed this record on November 20, 2014