Italian researchers launch Largest-Ever study on rare genetic condition in children
NCT ID NCT06723938
First seen Mar 21, 2026 · Last updated May 14, 2026 · Updated 7 times
Summary
This study looks at 520 children and teens with a rare condition called 46, XY DSD, where a person's chromosomes (XY) don't match their physical sex development. Researchers will collect genetic and physical information to better understand the condition. The goal is to learn more, not to test a new treatment.
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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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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.