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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
PTEN Hamartoma Tumor Syndrome Pediatric Patient RegistryCongenital 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, autism, autism spectrum disorder, central nervous system malformation, cerebral cortical dysplasia, hamartoma, hereditary disease, hereditary neoplastic syndrome, macrocephaly-autism syndrome, megalencephaly, musculoskeletal system disorder, neoplasm, nervous system disorder, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorderRecruitingNot stated2026-08-31NCT06462430

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Research sitesCityCountryLinked trials
Dr.Canan Kocaman pediatric clinicIstanbulTurkey (Türkiye)1