Scientists hunt for genetic clues behind baby thyroid condition
NCT ID NCT06728735
Summary
This study aims to understand the genetic causes of a lifelong thyroid condition present from birth, called congenital hypothyroidism. Researchers will analyze the genes of about 350 children and young adults in Italy who have this condition. The goal is to learn which genetic changes are most common, how they relate to the child's health, and what this means for families.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
RECRUITINGBologna, Bologna, 40138, Italy
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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