Characterization and Natural History of Williams Syndrome and Other Chromosome 7q11.23 Variants | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Characterization and Natural History of Williams Syndrome and Other Chromosome 7q11.23 Variants	Aortic Stenosis, Supravalvular, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Ventricular Outflow Obstruction, Williams syndrome, aortic valve disorder, aortic valve stenosis, autism, autism spectrum disorder, cardiovascular disorder, chromosomal disorder, heart disorder, heart valve disorder, hereditary disease, intellectual disability, nervous system disorder, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorder	Recruiting	Not stated	2026-06-08		NCT06930417

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Organizations	Linked trials
Children's Hospital of Philadelphia	215
University of Pennsylvania	502

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
University of Pennsylvania	Philadelphia	United States	507