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Sponsored by: |
Hadassah Medical Organization |
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Information provided by: | Hadassah Medical Organization |
ClinicalTrials.gov Identifier: | NCT00382369 |
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.
Condition |
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Vocal Cord Paralysis |
Study Type: | Observational |
Study Design: | Family-Based, Prospective |
Official Title: | Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis |
DNA prepared from blood
Estimated Enrollment: | 60 |
Study Start Date: | May 2005 |
Estimated Study Completion Date: | December 2007 |
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 was located on chromosome 6q16. We will be analyzing 2 extended families with familial vocal cord paralysis to define their genetic defect leading to the disease. All family members will undergo a laryngoscopy to determine the extent of paralysis. For all family members we will isolate DNA and determine their microsatellite polymorphism on chromosome 6q16. If the results are negative we will continue the study and perform a whole genome scan to localize the gene(s) involved.
Ages Eligible for Study: | 10 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Families suffering of familial vocal cord paralysis
Inclusion Criteria:
Exclusion Criteria:
Contact: Eitan Kerem, MD | 972-2-5844430 | kerem@hadassah.org.il |
Israel | |
Hadassah-Hebrew University Medical Center, Mt Scopus | Recruiting |
Jerusalem, Israel, 24035 | |
Contact: Arik Tzukert, DMD 00 972 2 6776095 arik@hadassah.org.il | |
Contact: Hadas Lemberg, PhD 00 972 2 6777572 lhadas@hadassah.org.il | |
Sub-Investigator: Ariela Simon, MD |
Study Director: | Eitan Kerem, MD | Hadassah MO |
Principal Investigator: | Batsheva Kerem, PhD | Hebrew University Jerusalem |
Responsible Party: | Hadassah Medical Organization ( Prof Eitan Kerem ) |
Study ID Numbers: | VOCALCORD-HMO-CTIL |
Study First Received: | September 28, 2006 |
Last Updated: | May 12, 2008 |
ClinicalTrials.gov Identifier: | NCT00382369 |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
familial vocal cord paralysis genetic screening |
Paralysis Signs and Symptoms Otorhinolaryngologic Diseases Respiratory Tract Diseases |
Vocal Cord Paralysis Neurologic Manifestations Laryngeal Diseases |
Vagus Nerve Diseases Nervous System Diseases Cranial Nerve Diseases |