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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Biochemical and Phenotypical Aspects of Smith-Lemli-Opitz Syndrome and Related Disorders of Cholesterol MetabolismAbnormalities, Multiple, CHILD syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Smith-Lemli-Opitz syndrome, desmosterolosis, hereditary disease, inborn errors of metabolism, lathosterolosis, metabolic disease, steroid inherited metabolic disorderRecruitingNot stated2026-08-17NCT05047354

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Research sitesCityCountryLinked trials
National Institutes of Health Clinical CenterBethesdaUnited States800