Scientists track rare family disease for clues to stop organ damage
NCT ID NCT00091871
Summary
This study aims to understand a rare, inherited condition called familial hypereosinophilia, where high levels of a specific white blood cell can damage organs over time. Researchers will follow about 50 family members, both with and without the condition, for many years with annual check-ups and blood tests. The goal is to learn how the disease progresses, find its genetic cause, and identify early warning signs before serious damage occurs.
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Contacts and locations
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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
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