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Intestinal Pseudo Obstruction

What is Intestinal Pseudo Obstruction?

Intestinal Pseudo Obstruction is a rare disorder characterized by the decreased ability of the intestines to push food through.

 

Intestinal Pseudo Obstruction is a rare disorder characterized by the decreased ability of the intestines to push food through.
Acknowledgement of Intestinal Pseudo Obstruction has not been added yet.
Prevalence Information of Intestinal Pseudo Obstruction has not been added yet.
Synonyms for Intestinal Pseudo Obstruction has not been added yet.
Cause of Intestinal Pseudo Obstruction has not been added yet.
Name Description
Abdominal pain Abdominal pain
Constipation Constipation
Diarrhea Diarrhea
Distended Stomach Distended Stomach
Diagnosis of Intestinal Pseudo Obstruction has not been added yet.
Diagnostic tests of Intestinal Pseudo Obstruction has not been added yet
Treatments of Intestinal Pseudo Obstruction has not been added yet.
Prognosis of Intestinal Pseudo Obstruction has not been added yet.
Tips or Suggestions of Intestinal Pseudo Obstruction has not been added yet.
References of Intestinal Pseudo Obstruction has not been added yet.
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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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