Nontuberculous Mycobacteria
What is Nontuberculous Mycobacteria?
Nontuberculous Mycobacteria is a bacteria that is found in water, some domestic and wild animals, and soil. NTM is a primary cause of respiratory disease in humans and is a leading cause of death in HIV/AIDS patients.
| Name | Description |
|---|---|
| Fever | Fever |
| Weight Loss | Weight Loss |
| Lack of appetite | Lack of appetite |
| Cough | Cough |
| Night Sweats | Night Sweats |
| Blood in the sputum | Blood in the sputum |
| Loss of energy | Loss of energy |
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| Title | Description | Date | Link |
|---|---|---|---|
| Stop NTM Now |
We are an online resource for Nontuberculous Mycobacteria (NTM). Our website will provide you with basic information about about NTMs, including symptoms, frequently asked questions, and methods of treatment. |
03/20/2017 | |
| The NTM Handbook |
The purpose of this website is to provide information about NTM to patients and their families. NTM is also known as atypical tuberculosis (Atypical TB) or mycobacteria other than tuberculosis (MOTT). |
03/20/2017 |
Clinical Trials
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.
- Complete the screening form.
- Review the informed consent.
- 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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