Scientists dig deeper into hidden DNA changes behind rare childhood disorders
NCT ID NCT07497477
First seen Apr 15, 2026 · Last updated May 01, 2026 · Updated 2 times
Summary
This study looks at people with rare genetic conditions called imprinting disorders, which can affect growth and development. Researchers want to find out how often extra DNA changes (called MLID) occur in these patients. They will test a new method to detect these changes in up to 96 participants, including healthy controls.
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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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Molecular Endocrinology and Imprinting disorder department - Trousseau Hospital
Paris, 75012, France
Contact Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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