NCT02699190
- Conditions
- 4H Syndrome, ADLD, AGS, +173 more
- Locations
-
- The Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States
Clinical trial condition
X-Linked Intellectual Disability
Explore clinical trials studying X-Linked Intellectual Disability. Study availability and eligibility vary by location and protocol.
271 public trials
52 recruiting studies
X-Linked Intellectual Disability trial results
Completed
NIPD on CFTC for Triplet Repeat Diseases
NCT03087526
- Conditions
- Ataxia, Basal Ganglia Diseases, Brain Diseases, +37 more
- Locations
-
- CHU Bordeaux Bordeaux, France
- CHU Montpellier Montpellier, France
- CHU Nice Nice, France
- CHU Nîmes Nîmes, France
Completed
Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
-
- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +23 more
- Locations
-
- Ann & Robert H Lurie Childrens Hospital of Chicago Chicago, Illinois, United States
- University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States
- Legacy Emanuel Hospital Portland, Oregon, United States
- Children's Hospital of Pittsburgh of UPMC Pittsburgh, Pennsylvania, United States
NCT03359213
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +16 more
- Locations
-
- Grupo de Pesquisa Clínica em Genética Médica - HCPA Porto Alegre, Brazil
- Igeim - Unifesp São Paulo, Brazil
NCT02412787
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +17 more
- Locations
-
- Children's Hospital and Research Center at Oakland Oakland, California, United States
- Ann & Robert H Lurie Children's Hospital of Chicago Chicago, Illinois, United States
- University of North Carolina Chapel Hill, North Carolina, United States
- Women's and Children's Hospital Adelaide, Australia
Completed
Neural Biomarkers in Fragile X Syndrome
NCT06957054
- Conditions
- Central Nervous System Diseases, Chromosome Disorders, Congenital Abnormalities, +20 more
- Locations
-
- Hospital del Mar Research Institute (HMRI) Barcelona, Spain
- Consorci Corporació Sanitaria Parc Taulí. Institut Investigació i Innovació Parc Taulí (I3PT) Sabadell, Barcelona, Spain
Completed
A Clinical Study to Evaluate the Efficacy and Safety of MIN-102 (IMP) in Male AMN Patients.
NCT03231878
- Conditions
- Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +21 more
- Locations
-
- Stanford University Medical Center Stanford, California, United States
- Kennedy Krieger Institute Baltimore, Maryland, United States
- Massachusetts General Hospital Boston, Massachusetts, United States
- Hospital de la Pitié-Salpêtrière Paris, France
NCT04571970
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +23 more
- Locations
-
- University of California San Francisco, Benioff Children's Hospital Oakland, California, United States
- McGill University Heath Center Montreal, Quebec, Canada
Completed
A Study of Elaprase in Children and Adults With Hunter Syndrome (Mucopolysaccharidosis II) in India
NCT05058391
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +17 more
- Locations
-
- SAT Hospital - Govt Medical College Thiruvananthapuram, Kerala, India
- JK Lone Hospital Jaipur, Rajasthan, India
- Institute of Child Health Kolkata, India
- All India Institute of Medical Sciences (AIIMS) New Delhi, India
Related conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (271)
- Heredodegenerative Disorders, Nervous System (267)
- Nervous System Diseases (265)
- Neurobehavioral Manifestations (264)
- Neurologic Manifestations (263)
- Genetic Diseases, X-Linked (261)
- Genetic Diseases, Inborn (260)
- Intellectual Disability (260)