desmosterolosis

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Biochemical and Phenotypical Aspects of Smith-Lemli-Opitz Syndrome and Related Disorders of Cholesterol Metabolism	Abnormalities, 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 disorder	Recruiting	Not stated	2026-08-17		NCT05047354

Clinical trials