Scientists seek families with rare blood disorder to unlock genetic secrets
NCT ID NCT03854318
First seen Nov 01, 2025 · Last updated May 12, 2026 · Updated 26 times
Summary
This study follows people of any age who have or may have a RUNX1 gene change, which can cause bleeding problems and increase the risk of blood cancers. Researchers will collect medical history, blood samples, and sometimes bone marrow over many years to learn how the condition develops. The goal is to improve diagnosis, monitoring, and future treatments for these rare inherited blood disorders.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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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
Explore the condition pages connected to this study.