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Asperger Syndrome

What is Asperger Syndrome?

Asperger Syndrome is characterized by difficulties in social interaction and restricted patterns of behavior and interests.

 

Asperger Syndrome is characterized by difficulties in social interaction and restricted patterns of behavior and interests.
Acknowledgement of Asperger Syndrome has not been added yet.
Prevalence Information of Asperger Syndrome has not been added yet.
Synonyms for Asperger Syndrome has not been added yet.
Cause of Asperger Syndrome has not been added yet.
Symptoms for Asperger Syndrome has not been added yet.
Diagnosis of Asperger Syndrome has not been added yet.
Diagnostic tests of Asperger Syndrome has not been added yet
Treatments of Asperger Syndrome has not been added yet.
Prognosis of Asperger Syndrome has not been added yet.
Tips or Suggestions of Asperger Syndrome has not been added yet.
References of Asperger Syndrome has not been added yet.
Hello Everyone Created by Nimonic
Last updated 10 Sep 2016, 10:00 PM

Posted by Nimonic
7 Sep 2016, 09:07 PM

I was diagnosed with Atypical Autism as a child and later with Asperger's Syndrome. I also have OCA2(Albinism), Spinal Muscular Atrophy, and Complete Androgen Insensitivity Syndrome. I do have other health problems as a result of injuries from prior work I did.

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Cords registry

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.
  2. Review the informed consent.
  3. Answer the permission and data sharing questions.

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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Hi I'm a mom to 5 kids and 3 of which have various medical conditions my 6 year old daughter has tapvr mixed and we didn't know at all and she almost passed at birth she's having some...

Hi I'm a mom to 5 kids and 3 of which have various medical conditions my 6 year old daughter has tapvr mixed and we didn't know at all and she almost passed at birth she's having some...

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My profile can wait
My husband and my youngest son both have Asperger's Syndrome.

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Hello Everyone

Created by Nimonic | Last updated 10 Sep 2016, 10:00 PM


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