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Loose Anagen Hair Syndrome

What is Loose Anagen Hair Syndrome ?

Loose Anagen Hair Syndrome is a rare disorder in which hair falls out easily and is pulled out easily.

 

Loose Anagen Hair Syndrome is a rare disorder in which hair falls out easily and is pulled out easily.
Acknowledgement of Loose Anagen Hair Syndrome has not been added yet.
Prevalence Information of Loose Anagen Hair Syndrome has not been added yet.
Synonyms for Loose Anagen Hair Syndrome has not been added yet.
Cause of Loose Anagen Hair Syndrome has not been added yet.
Symptoms for Loose Anagen Hair Syndrome has not been added yet.
Diagnosis of Loose Anagen Hair Syndrome has not been added yet.
Diagnostic tests of Loose Anagen Hair Syndrome has not been added yet
Treatments of Loose Anagen Hair Syndrome has not been added yet.
Prognosis of Loose Anagen Hair Syndrome has not been added yet.
Tips or Suggestions of Loose Anagen Hair Syndrome has not been added yet.
References of Loose Anagen Hair Syndrome has not been added yet.
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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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Community User List

Dr. Ryan Wade, D.C. is a Board Certified Chiropractic Physician, Physiotherapist with a background in Personal Fitness and Sports Nutrition that is also liscensed to perform manipulation under...
My daughter is almost 3 years old and we have been told that she is likely to be suffering from LAS. About 2 months ago I noticed loose hair in her bed, at first I didn't worry as she had lovely...
I am a Stay at home mom to two fantastic girls. One of whom was just dxed with the Noonans syndrome with loose anagon hair...SHOC2 gene mutation. I have heard it has a great prognosis.
I am 28 and have three girls. The oldest is almost 7 and still has problems with the loose anagen syndrome.
I am a concerned mother of a 3 1/2 year old daugher with Loose Anagen Hair Syndrome.

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