Scientists decode fetal DNA to unlock secrets of rare birth defects
NCT ID NCT06475651
First seen Mar 28, 2026 · Last updated May 15, 2026 · Updated 4 times
Summary
This study looks at DNA methylation patterns (chemical tags on DNA) in fetal tissue and amniotic fluid to help diagnose rare genetic diseases that start before birth. Researchers will compare these patterns with those from children's blood to see if they differ. The goal is to improve how doctors identify these conditions, not to treat them directly.
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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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Department of Genomic Medicine for Rare Diseases and the Multidisciplinary Center for Prenatal Diagnosis of the Necker-Enfants malades Hospital
RECRUITINGParis, 75015, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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