polymicrogyria
polymicrogyria
Explore linked clinical trials. Standard reference: MONDO:00000872 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Brain Development Research Program | Aicardi 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 disorder | Recruiting | Not stated | 2026-08-17 | NCT00305305 | |
| Human Epilepsy Genetics--Neuronal Migration Disorders Study | Choristoma, Cognition Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Malformations of Cortical Development, Group I, Malformations of Cortical Development, Group II, Malformations of Cortical Development, Group III, Musculoskeletal Abnormalities, Neurologic Manifestations, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, cognitive disorder, epilepsy, lissencephaly spectrum disorders, microcephaly, musculoskeletal system disorder, nervous system disorder, polymicrogyria, psychiatric disorder, schizencephaly, visual epilepsy | Recruiting | Not stated | 2023-09-21 | NCT00041600 |