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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Optical Imaging in X-linked Disorders.Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Sex Chromosome Disorders, X-linked disease, chromosomal disorder, creatine transporter deficiency, fragile X syndrome, hereditary disease, inherited neurodegenerative disorder, intellectual disability, nervous system disorderRecruitingNot applicable2026-05-15NCT06868979

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OrganizationsLinked trials
Hospices Civils de Lyon429

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Research sitesCityCountryLinked trials
Woman, mother and child hospital, Hospices Civils de LyonBronFrance2