NCT00041600
- Conditions
- Brain Diseases, Brain Malformation, Central Nervous System Diseases, +27 more
- Locations
-
- Boston Children's Hospital, Walsh Laboratory Boston, Massachusetts, United States
Clinical trial condition
Malformations of Cortical Development
Explore clinical trials studying Malformations of Cortical Development. Study availability and eligibility vary by location and protocol.
127 public trials
34 recruiting studies
Malformations of Cortical Development trial results
Recruiting
GROWing Up With Rare GENEtic Syndromes
NCT04463316
- Conditions
- 17p- Deletiesyndrome, 1q25-32 Deletie, 22q11 Deletion Syndrome, +138 more
- Locations
-
- Erasmus Medical Center Rotterdam, South Holland, Netherlands
NCT05534672
- Conditions
- Brain Diseases, Central Nervous System Diseases, Congenital Abnormalities, +17 more
- Locations
-
- Medical University of Lodz Lodz, Poland
- Children's Memorial Health Institute, Neurology and Epileptology Warsaw, Poland
NCT01403402
- Conditions
- Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations), Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy), Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan), +89 more
- Locations
-
- Congenital Muscle Disease International Registry (www.cmdir.org) Lakewood, California, United States
Not yet recruiting
A Phase 2 Study of the Safety and Efficacy of AV078 in Participants With Tuberous Sclerosis Complex (TSC) Refractory Epilepsy
NCT07680322
- Conditions
- Brain Diseases, Central Nervous System Diseases, Congenital Abnormalities, +21 more
- Locations
-
Not specified
Not yet recruiting
Fluorescence Guided Focal Cortical Dysplasia Surgery
NCT07657975
- Conditions
- Brain Diseases, Central Nervous System Diseases, Congenital Abnormalities, +8 more
- Locations
-
- Hôpital Neurologique Pierre Wertheimer - Groupement Hospitalier Est - Hospices Civils de Lyon Bron, France
- Hôpital Femme Mère Enfant - Groupement Hospitalier Est - Hospices Civils de Lyon Bron, France
Not yet recruiting
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk
NCT07142772
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, +9 more
- Locations
-
- service Génétique clinique Pitié-Salpêtrière / Trousseau Paris, France
Enrolling by invitation
Parent and Infant Inter(X)Action Intervention (PIXI)
NCT03836300
- Conditions
- 22q11 Deletion Syndrome, Abnormalities, Multiple, Angelman Syndrome, +81 more
- Locations
-
- RTI International Research Triangle Park, North Carolina, United States
Enrolling by invitation
TANDem-2: Closing the Gap to Interventions for TAND
NCT06879665
- Conditions
- Adult Caregivers of Individuals With TSC, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +14 more
- Locations
-
- TSC Alliance Silver Spring, Maryland, United States
- Tuberous Sclerosis Australia Beverly Hills, New South Wales, Australia
Enrolling by invitation
Reproductive Options in Inherited Skin Diseases
NCT06330324
- Conditions
- Abnormalities, Multiple, Albinism, Amino Acid Metabolism, Inborn Errors, +56 more
- Locations
-
- Maastricht University Medical Center Maastricht, Limburg, Netherlands
Related conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (127)
- Nervous System Diseases (126)
- Nervous System Malformations (126)
- Congenital Abnormalities (122)
- Malformations of Cortical Development, Group I (121)
- Genetic Diseases, Inborn (96)
- Heredodegenerative Disorders, Nervous System (90)
- Neurodegenerative Diseases (90)