500 families join quest to solve mystery of fetal hydrops
NCT ID NCT03412760
First seen Feb 05, 2026 · Last updated May 20, 2026 · Updated 13 times
Summary
This study aims to uncover the genetic reasons behind non-immune hydrops fetalis (a severe fetal condition) and other birth defects. Researchers will use advanced genetic testing (exome sequencing) on 500 affected fetuses or newborns to find hidden genetic causes. The goal is to better understand these conditions 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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Contacts and locations
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Locations
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University of California, San Francisco
San Francisco, California, 94143, United States
Conditions
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