Scientists search for genetic clues behind rare facial paralysis condition
NCT ID NCT02055248
Summary
This study aimed to better understand Moebius syndrome and related disorders where people are born with facial weakness. Researchers examined 207 participants and their family members to document symptoms and look for genetic causes. The goal was to gather detailed information to improve diagnosis and provide better guidance to affected families.
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Contacts and locations
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Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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