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Superior Canal Dehiscence Syndrome

What is Superior Canal Dehiscence Syndrome?

Superior Canal Dehiscence Syndrome is a rare medical condition of the inner ear leading to hearing and balance disorders in those affected. Symptoms are caused by a thinning or absence of the part of the temporal bone overlying the superior semicircular canal of the vestibular system. It may result from slow erosion of the bone or physical trauma to the skull and there is evidence that the defect or susceptibility is congenital.

 

Superior Canal Dehiscence Syndrome is a rare medical condition of the inner ear leading to hearing and balance disorders in those affected. Symptoms are caused by a thinning or absence of the part of the temporal bone overlying the superior semicircular canal of the vestibular system. It may result from slow erosion of the bone or physical trauma to the skull and there is evidence that the defect or susceptibility is congenital.
Acknowledgement of Superior Canal Dehiscence Syndrome has not been added yet.
Prevalence Information of Superior Canal Dehiscence Syndrome has not been added yet.
Synonyms for Superior Canal Dehiscence Syndrome has not been added yet.
Cause of Superior Canal Dehiscence Syndrome has not been added yet.
Symptoms for Superior Canal Dehiscence Syndrome has not been added yet.
Diagnosis of Superior Canal Dehiscence Syndrome has not been added yet.
Diagnostic tests of Superior Canal Dehiscence Syndrome has not been added yet
Treatments of Superior Canal Dehiscence Syndrome has not been added yet.
Prognosis of Superior Canal Dehiscence Syndrome has not been added yet.
Tips or Suggestions of Superior Canal Dehiscence Syndrome has not been added yet.
References of Superior Canal Dehiscence Syndrome has not been added yet.
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CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access.

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After these steps, the enrollment process is complete. All other questions are voluntary. However, these questions are important to patients and their families to create awareness as well as to researchers to study rare diseases. This is why we ask our participants to update their information annually or anytime changes to their information occur.

Researchers can contact CoRDS to determine if the registry contains participants with the rare disease they are researching. If the researcher determines there is a sufficient number of participants or data on the rare disease of interest within the registry, the researcher can apply for access. Upon approval from the CoRDS Scientific Advisory Board, CoRDS staff will reach out to participants on behalf of the researcher. It is then up to the participant to determine if they would like to join the study.

Visit sanfordresearch.org/CoRDS to enroll.

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