progressive myoclonic epilepsy type 3

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History and Longitudinal Clinical Assessments in NCL / Batten Disease, the International DEM-CHILD Database	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Kufor-Rakeb syndrome, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Neuronal Ceroid-Lipofuscinoses, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, inherited neurodegenerative disorder, juvenile neuronal ceroid lipofuscinosis, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, neurodegenerative disease, neuronal ceroid lipofuscinosis 1, neuronal ceroid lipofuscinosis 5, parkinsonism due to ATP13A2 deficiency, progressive myoclonic epilepsy type 3	Recruiting	Not stated	2021-10-29		NCT04613089

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