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Introduction: Williams-Beuren syndrome is a rare genetic disorder caused by a 7q11.23 microdeletion. The phenotype associates vasculopathy (arterial stenosis, hypertension), dimorphism and intellectua...
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Lead Sponsor
Hospices Civils de Lyon
NCT04770012 · Cardiac Allograft Vasculopathy, Heart Transplant
NCT02798731 · Cardiac Allograft Vasculopathy
NCT05826444 · Cardiac Allograft Vasculopathy
NCT04463316 · Prader-Willi Syndrome, PWS-like Syndrome, and more
NCT03386539 · Pediatric Heart Transplantation, Immunosuppression, and more
Hôpital Femme Mère Enfant - Hospices Civils de Lyon
Bron
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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