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Essential Thrombocythemia

What is Essential Thrombocythemia?

Essential Thrombocythemia is a rare chronic blood disorder characterized by the overproduction of platelets.

 

Essential Thrombocythemia is a rare chronic blood disorder characterized by the overproduction of platelets.
Acknowledgement of Essential Thrombocythemia has not been added yet.
27.5http://www.orpha.net
Synonyms for Essential Thrombocythemia has not been added yet.
Cause of Essential Thrombocythemia has not been added yet.
Symptoms for Essential Thrombocythemia has not been added yet.
Diagnosis of Essential Thrombocythemia has not been added yet.
Diagnostic tests of Essential Thrombocythemia has not been added yet
Treatments of Essential Thrombocythemia has not been added yet.
Prognosis of Essential Thrombocythemia has not been added yet.
Tips or Suggestions of Essential Thrombocythemia has not been added yet.
References of Essential Thrombocythemia has not been added yet.
Essential thrombocythemia Created by Ladydi
Last updated 1 Apr 2015, 07:54 AM

Posted by Ladydi
1 Apr 2015, 07:54 AM

I have just been diagnosed with essential thrombocythemia and am looking for others who can give me some information about this disorder. I am particularly interested in finding out about treatments and the drug Hydroxyurea.

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MPNConnect

MPNConnect supports people living with myeloproliferative neoplasms (MPNs), caregivers, family members and others in the community. The website's goal is to help improve your knowledge of myeloproliferative neoplasms.

03/20/2017

Clinical Trials


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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Essential thrombocythemia

Created by Ladydi | Last updated 1 Apr 2015, 07:54 AM


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