Natural History Study of Individuals With Autism and Germline Heterozygous PTEN Mutations | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History Study of Individuals With Autism and Germline Heterozygous PTEN Mutations	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cowden disease, Craniofacial Abnormalities, Malformations of Cortical Development, Group I, Musculoskeletal Abnormalities, Neoplasms, Multiple Primary, PTEN hamartoma tumor syndrome, atrial septal defect, autism, autism spectrum disorder, central nervous system malformation, cerebral cortical dysplasia, hamartoma, hereditary disease, hereditary neoplastic syndrome, megalencephaly, musculoskeletal system disorder, neoplasm, nervous system disorder, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorder	Active, not recruiting	Not stated	2026-08-06		NCT02461446

6 results · Page 1 of 1

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Organizations	Linked trials
Boston Children's Hospital	238
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)	536
National Center for Advancing Translational Sciences (NCATS)	127
National Institute of Neurological Disorders and Stroke (NINDS)	370
National Institutes of Health (NIH)	667
Office of Rare Diseases (ORD)	7

5 results · Page 1 of 1

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Research sites	City	Country	Linked trials
Boston Children's Hospital	Boston	United States	343
Cincinnati Children's Hospital Medical Center	Cincinnati	United States	405
Cleveland Clinic	Cleveland	United States	558
Stanford University Medical Center	Stanford	United States	43
University of California at Los Angeles	Los Angeles	United States	14