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Paroxysmal Kinesigenic Dyskinesia

What is Paroxysmal Kinesigenic Dyskinesia ?

Paroxysmal Kinesigenic Dyskinesia is a rare neurological disorder characterized by short, recurring attacks of involuntary movement, triggered by sudden voluntary movement.

 

Paroxysmal Kinesigenic Dyskinesia is a rare neurological disorder characterized by short, recurring attacks of involuntary movement, triggered by sudden voluntary movement.
Acknowledgement of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Prevalence Information of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Synonyms for Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Cause of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Symptoms for Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Diagnosis of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Diagnostic tests of Paroxysmal Kinesigenic Dyskinesia has not been added yet
Treatments of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Prognosis of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
Tips or Suggestions of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
References of Paroxysmal Kinesigenic Dyskinesia has not been added yet.
a place to say hi and introduce youself Created by Jgmbravesfan
Last updated 16 May 2012, 03:41 AM

Posted by Megzy
16 May 2012, 03:41 AM

Hello, I'm not sure if anyone is on here anymore, but my name is Meghan and I developed PKD and PKND when I was 22. My condition has continued to increase in new symptoms. I wanted to find others to talk to and see if they have any advice on how they deal with their symptoms.

Posted by Jgmbravesfan
29 Jul 2010, 03:39 AM

I guess I'll start thing off. I'm John, I'm 22, I'm from South Carolina and I was diagnose with PKC when I was 13.

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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.

Enrolling is easy.

  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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a place to say hi and introduce youself

Created by Jgmbravesfan | Last updated 16 May 2012, 03:41 AM


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