New study aims to unlock secrets of infections in rare mitochondrial disease
NCT ID NCT04419870
First seen May 01, 2026 · Last updated May 24, 2026 · Updated 3 times
Summary
This study looks at how infections affect people with mitochondrial disease, a rare genetic disorder that can cause muscle weakness and developmental delays. Researchers will collect blood samples and health data from 400 participants and their family members to find immune patterns linked to severe illness. The goal is to better understand these infections and identify ways to improve treatment.
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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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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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