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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Brain Development Research ProgramAicardi syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Malformations of Cortical Development, Group III, Neurobehavioral Manifestations, Neurologic Manifestations, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, X-linked disease, autism, autism spectrum disorder, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, corpus callosum, agenesis of, epilepsy, eye disorder, hereditary disease, intellectual disability, nervous system disorder, neurodevelopmental disorder, pervasive developmental disorder, polymicrogyria, psychiatric disorderRecruitingNot stated2026-08-17NCT00305305

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Research sitesCityCountryLinked trials
University of California, San FranciscoSan FranciscoUnited States294