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Hyperhidrosis

What is Hyperhidrosis?

Hyperhidrosis is a rare disorder characterized by excessive sweating on the palms of the hands, the soles of the feet, in the armpits, in the groin area, and/or under the breasts.

 

Hyperhidrosis is a rare disorder characterized by excessive sweating on the palms of the hands, the soles of the feet, in the armpits, in the groin area, and/or under the breasts.
Acknowledgement of Hyperhidrosis has not been added yet.
Prevalence Information of Hyperhidrosis has not been added yet.
Synonyms for Hyperhidrosis has not been added yet.
The cause of Primary Hyperhidrosis is unknown. A disorder of the thyroid or pituitary gland, diabetes mellitus, tumors, gout, menopause, certain drugs, or mercury poisoning can lead to Secondary Hyperhidrosis.
Name Description
Excessive sweating excessive sweating
Diagnosis of Hyperhidrosis has not been added yet.
Diagnostic tests of Hyperhidrosis has not been added yet
Treatments of Hyperhidrosis has not been added yet.
Prognosis of Hyperhidrosis has not been added yet.
Tips or Suggestions of Hyperhidrosis has not been added yet.
References of Hyperhidrosis has not been added yet.
Don't want to be the only one Created by Defaziosm
Last updated 9 Apr 2013, 06:28 AM

Posted by Defaziosm
9 Apr 2013, 06:28 AM

I would like to talk to others who have Hyperhydrosis. I know I'm not the only one but I'm tired of feeling like I am. I look forward to hearing from you.

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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.
  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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Don't want to be the only one

Created by Defaziosm | Last updated 9 Apr 2013, 06:28 AM


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