Baby blood tests could catch hidden cholesterol disorder
NCT ID NCT07470723
First seen Mar 14, 2026 · Last updated Jun 15, 2026 · Updated 12 times
Summary
This study aims to find different types of familial hypercholesterolemia (FH) in newborns. Parents give a cheek swab for genetic testing, and babies provide 5 blood samples over 2 years. The goal is to improve early detection and understanding of this inherited high-cholesterol condition.
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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
Email: •••••@•••••
Locations
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University of Wisconsin - Madison
RECRUITINGMadison, Wisconsin, 53792, United States
Contact Email: •••••@•••••
Conditions
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