Not Signed In -
Spondyloepiphyseal dysplasia congenita |
SED congenita; SEDc |
Clinical Trial: Pilot Study of Familial Nonsyndromal Mondini Dysplasia
This study has been completed.
|
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.
| Condition |
|---|
| Mondini dysplasia |
MedlinePlus related topics: Ear Disorders
Study Type: Observational
Study Design: Screening
Further Study Details:
Expected Total Enrollment: 2
Study start: October 1995
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.
Eligibility
Genders Eligible for Study: Both
Criteria
PROTOCOL ENTRY CRITERIA: Parents of a study family with nonsyndromal Mondini dysplasia
Location Information
Michigan
University of Michigan Health Systems, Ann Arbor, Michigan, 48109, United States
Study chairs or principal investigators
Andrew J. Griffith, Study Chair, University of Michigan
More Information
Study ID Numbers: 199/11895; UMMC-1402
Record last reviewed: April 2002
Last Updated: October 13, 2004
Record first received: October 18, 1999
ClinicalTrials.gov Identifier: NCT00004336
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Record last reviewed: April 2002
Last Updated: October 13, 2004
Record first received: October 18, 1999
ClinicalTrials.gov Identifier: NCT00004336
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Genetics Home Reference: Spondyloepiphyseal dysplasia congenita (Genetics Home Reference)
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