Scientists hunt for genetic clues to rare childhood heart conditions
NCT ID NCT05330338
Summary
This study aims to discover the genetic causes of two rare, complex heart defects present at birth. Researchers will analyze DNA from about 600 children with these conditions and their parents to find new genetic links. The goal is to build knowledge that could lead to better, more personalized diagnosis and management for future patients.
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Contacts and locations
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Locations
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CHU Angers
Angers, Maine-et-Loire, 49000, France
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CHU Bordeaux
Bordeaux, Gironde, 33000, France
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CHU Lyon
Lyon, Rhône, 69000, France
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CHU Marseille
Marseille, Bouches-du-Rhône, 13000, France
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CHU Nancy
Nancy, Meurthe-et-Moselle, 54000, France
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CHU Nantes
Nantes, Loire-Atlantique, 44000, France
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CHU Rennes
Rennes, Brittany Region, 35000, France
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CHU Rouen
Rouen, Seine-Maritime, 76000, France
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CHU Toulouse
Toulouse, Haute-Garonne, 31000, France
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CHU Tours
Tours, Val de Loire, 37000, France
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CHU de Caen
Caen, Normandy, 14000, France
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CHU de Lille
Lille, Hauts-de-France, 59000, France
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Groupe Hospitalier St Joseph - Hôpital Marie Lannelongue
Le Plessis-Robinson, Hauts-de-Seine, 92350, France
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Hôpital Européen Georges Pompidou
Paris, Paris, 75000, France
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Hôpital Nord Laennec
Saint-Herblain, Loire-Atlantique, 44093, France
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Intercard Lille
Lille, Nord, 59000, France
Conditions
Explore the condition pages connected to this study.