10,000 families join hunt for hidden genes behind rare diseases
NCT ID NCT02743845
First seen Apr 05, 2026 · Last updated May 23, 2026 · Updated 7 times
Summary
This study enrolls people with rare or undiagnosed conditions, along with their family members, to find the genetic causes of their illnesses. Researchers collect DNA samples and medical information to analyze genes and identify disease-causing changes. If a genetic cause is found, it is shared with the family through their doctor. The goal is to improve diagnosis and future treatments for rare diseases.
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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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.