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Tourette Syndrome

What is Tourette Syndrome?

Tourette Syndrome is an genetic neuropsychiatric disorder characterized by multiple physical tics and at least one vocal tic.

 

Tourette Syndrome is an genetic neuropsychiatric disorder characterized by multiple physical tics and at least one vocal tic.
Acknowledgement of Tourette Syndrome has not been added yet.
Prevalence Information of Tourette Syndrome has not been added yet.
Synonyms for Tourette Syndrome has not been added yet.
Cause of Tourette Syndrome has not been added yet.
Symptoms for Tourette Syndrome has not been added yet.
Diagnosis of Tourette Syndrome has not been added yet.
Diagnostic tests of Tourette Syndrome has not been added yet
Treatments of Tourette Syndrome has not been added yet.
Prognosis of Tourette Syndrome has not been added yet.
Tips or Suggestions of Tourette Syndrome has not been added yet.
References of Tourette Syndrome has not been added yet.
mother of 11 year old son with tourettes Created by susanfv
Last updated 11 Jun 2017, 02:42 AM

Posted by graychan
11 Jun 2017, 02:42 AM

I came across a nice news article on Tourette syndrome:  Tourette syndrome:  Finally something to shout about, www.chinapost.com.tw.

Posted by susanfv
1 Aug 2011, 04:06 AM

I am the mother of an exceptionally bright 11 year old boy with Tourettes, sensory integration disorder,( severe eating disorder secondary to sensory integration) Aspergers, ADD and OCD, and was interested in communicating with other parents who have children with this syndrome.I am especially curious if other children have similar medical issues along side the tourettes.

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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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  1. Complete the screening form.
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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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mother of 11 year old son with tourettes

Created by susanfv | Last updated 11 Jun 2017, 02:42 AM


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