Status:
COMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis
Lead Sponsor:
Hadassah Medical Organization
Conditions:
Vocal Cord Paralysis
Eligibility:
All Genders
10+ years
Brief Summary
Vocal cord paralysis is a common cause of congenital stridor and airway obstruction. In this study we plan to identify the genetic locus of the genes in two extended families who suffer of the disease...
Detailed Description
In a number of families suffering of familial vocal cord paralysis it has previously been shown that the disease is inherited autosomal dominant. In one of the families the gene coding for the disease...
Eligibility Criteria
Inclusion
- members of families suffering of familial vocal cord paralysis
Exclusion
- none
Key Trial Info
Start Date :
June 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 29 2008
Estimated Enrollment :
11 Patients enrolled
Trial Details
Trial ID
NCT00382369
Start Date
June 1 2008
End Date
December 29 2008
Last Update
February 27 2017
Active Locations (1)
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1
Hadassah-Hebrew University Medical Center, Mt Scopus
Jerusalem, Israel, 24035