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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Patterns of Neurodevelopmental DisordersAbnormalities, Multiple, Brain Diseases, Metabolic, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Down syndrome, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, PANDAS, autism spectrum disorder, brain disorder, central nervous system disorder, cerebral folate deficiency, chromosomal disorder, epilepsy, hereditary disease, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, intellectual disability, metabolic disease, mitochondrial encephalomyopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neurodegenerative syndrome due to cerebral folate transport deficiency, neurodevelopmental disorder, neuromuscular disease, pediatric acute-onset neuropsychiatric syndrome, pervasive developmental disorder, psychiatric disorderRecruitingNot stated2026-04-16NCT06213090

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Research sitesCityCountryLinked trials
Rossignol Medical CenterPhoenixUnited States2