peroxisome biogenesis disorder

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)	Abnormalities, Multiple, Bone Diseases, Developmental, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Peroxisomal Disorders, Urogenital Diseases, Zellweger spectrum disorders, adult Refsum disease, alpha-methylacyl-CoA racemase deficiency, bone disorder, brain disorder, central nervous system disorder, central nervous system malformation, chondrodysplasia punctata, d-bifunctional protein deficiency, hereditary disease, hereditary motor and sensory neuropathy, inborn errors of metabolism, inherited neurodegenerative disorder, kidney disorder, liver disorder, metabolic disease, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, osteochondrodysplasia, peripheral nervous system disorder, peroxisomal acyl-CoA oxidase deficiency, peroxisome biogenesis disorder, polyneuropathy, rhizomelic chondrodysplasia punctata, rhizomelic chondrodysplasia punctata type 1, sterol carrier protein 2 deficiency, urinary system disorder	Recruiting	Not stated	2025-12-10		NCT01668186

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