Scientists track rare disease to uncover genetic clues
NCT ID NCT00668291
Summary
This study aimed to better understand the symptoms and genetic causes of two rare conditions: Carney Complex and Primary Pigmented Nodular Adrenocortical Disease (PPNAD). Researchers followed 133 patients for three years, performing regular check-ups and genetic testing. The goal was to see how specific gene changes relate to the different symptoms people experience.
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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
Locations
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Hôpital Cochin
Paris, 75679, France
Conditions
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