Scientists hunt for clues to predict heart risk in rare fabry disease
NCT ID NCT07351136
First seen Jan 29, 2026 · Last updated May 01, 2026 · Updated 10 times
Summary
This study aims to find new ways to detect and predict heart problems in people with Fabry disease, a rare genetic condition. Researchers will analyze heart tissue samples and blood from 20 adult patients to look for specific proteins, genetic markers, and use a special PET scan to see heart scarring. The goal is to better understand how the heart is damaged and improve future diagnosis and care.
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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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