Scientists track rare blood disease across generations to unlock cancer clues
NCT ID NCT03854318
Summary
This study aims to learn more about a rare, inherited blood disorder called FPDMM, which is caused by a change in the RUNX1 gene. Researchers will follow people with this gene change and their family members over many years to understand how the disease develops, why some people get blood cancer, and to look for better ways to monitor and treat it. The study involves yearly check-ups, blood tests, and sample collection to track health changes over time.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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