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 who have this condition to see which genetic changes are most common. The goal is to improve diagnosis and provide better information to families about the condition's cause and risk of recurrence.
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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: •••••@•••••
Locations
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
RECRUITINGBologna, Bologna, 40138, Italy
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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