Major italian study aims to map the landscape of a rare congenital condition
NCT ID NCT06723938
Summary
This study aims to gather detailed information about children and adolescents diagnosed with 46,XY DSD, a rare condition where a person's chromosomes, internal reproductive organs, and physical appearance develop in a disharmonious way. Researchers will collect and analyze medical, hormonal, and genetic data from 520 patients across multiple Italian hospitals. The goal is to better describe the condition, understand how genetic findings relate to physical features, and improve future diagnosis and care.
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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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Azienda Ospedaliero Universitaria Pisana
NOT_YET_RECRUITINGPisa, Pisa, 56126, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
RECRUITINGBologna, Bologna, 40138, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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IRCCS Ospedale San Raffaele
NOT_YET_RECRUITINGMilan, Milano, 20132, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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Ospedale Pediatrico Bambino Gesù
NOT_YET_RECRUITINGRoma, Roma, 00165, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Conditions
Explore the condition pages connected to this study.