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| Sponsor: | National Institute on Deafness and Other Communication Disorders (NIDCD) |
|---|---|
| Information provided by: | National Institutes of Health Clinical Center (CC) |
| ClinicalTrials.gov Identifier: | NCT00023036 |
Purpose
This study will try to identify and understand the genetic factors that lead to inner ear malformation called "enlarged vestibular aqueducts", that can lead to hearing loss.
Patients with sensorineural hearing loss with or without inner ear malformations and their parents and siblings may be eligible for this study. Participants and their immediate family members, may undergo some or all of the following tests and procedures:
| Condition |
|---|
|
Sensorineural Hearing Loss Cytomegalovirus Infection |
| Study Type: | Observational |
| Official Title: | Clinical and Molecular Analysis of Enlarged Vestibular Aqueducts |
| Estimated Enrollment: | 500 |
| Study Start Date: | August 2001 |
Nonsyndromic hereditary hearing impairment is a genetically heterogeneous disorder that can be caused by mutations in any one of at least 60 different genes. Enlargement of the vestibular aqueduct (EVA) is a radiologic finding known to be associated with mutations in one of these genes, the Pendred syndrome gene (PDS). EVA may thus serve as a clinically useful marker to facilitate the diagnosis of hearing impairment. Recent data from our laboratory and others indicates that only a subset of individuals with EVA have PDS mutations, and therefore some EVA cases are likely to be caused by other genes, nongenetic factors, or a combination of these etiologies. Individuals with hearing impairment and EVA will be enrolled in this study in order to: (1) Prospectively determine the prevalence of PDS mutation in EVA patients; (2) correlate phenotypic features with PDS genotype status; 3) identify other genetic factors that cause EVA. Siblings and parents may also be enrolled in order to define inheritance and to perform molecular genetic analyses.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Subjects must have or be a family member of a participant with known or non-syndromic SNHL associated with inner ear malformations
For familial cases, there must be at least two participating affected family members; this to be treated as part of the familial sub-study, otherwise the subjects will be treated as individual, sporadic cases.
Adults must be able to provide informed consent
Minors must have a parent or guardian able to provide consent
Age between 0-99.
EXCLUSION CRITERIA:
Subjects with known exposure to physical or chemical teratogens in utero that could account for their inner ear malformations such as thalidomide or radiation
Any hearing loss that is associated with syndromes, such as, branchio-oto-renal (BOR) syndrome, which comprises system malformations and branchial cleft abnormalities and is caused by heterozygous mutations in the EYA1 gene.
Contacts and Locations| Contact: Patient Recruitment and Public Liaison Office | (800) 411-1222 | prpl@mail.cc.nih.gov |
| Contact: TTY | 1-866-411-1010 |
| United States, Maryland | |
| National Institutes of Health Clinical Center, 9000 Rockville Pike | Recruiting |
| Bethesda, Maryland, United States, 20892 | |
| Sub-Investigator: Patient Recruitment and Public Liaison Office (PRPL) For more information at the NIH Clinical Center contact | |
More Information
| ClinicalTrials.gov Identifier: | NCT00023036 History of Changes |
| Other Study ID Numbers: | 010228, 01-DC-0228 |
| Study First Received: | August 21, 2001 |
| Last Updated: | December 31, 2011 |
| Health Authority: | United States: Federal Government |
|
Genetics Deafness EVA Pendred Hearing |
Hearing Impairment Nonsyndromic Hereditary Hearing Impairment SNHL Inner Ear Enlarged Vestibular Aqueducts |
|
Cytomegalovirus Infections Hearing Loss Deafness Hearing Loss, Sensorineural Herpesviridae Infections DNA Virus Infections Virus Diseases |
Hearing Disorders Ear Diseases Otorhinolaryngologic Diseases Sensation Disorders Neurologic Manifestations Nervous System Diseases Signs and Symptoms |