Movement Disorders and Neurometabolic Diseases

dc.contributor.authorChristensen, Celanie K.
dc.contributor.authorWalsh, Laurence
dc.contributor.departmentNeurology, School of Medicineen_US
dc.date.accessioned2018-03-23T18:31:59Z
dc.date.available2018-03-23T18:31:59Z
dc.date.issued2018
dc.description.abstractMany inherited metabolic disorders cause movement disorders in children. This review focuses on chorea, dystonia, myoclonus, tremor, and parkinsonism. Broad categories commonly responsible for pediatric movement disorders include mitochondrial disorders, organic acidemias, mineral metabolism and transport disorders, neurotransmitter diseases, purine metabolism disorders, lipid storage disorders, and disorders of creatine metabolism. Each movement disorder can be caused by many different inherited metabolic disorders and several of the inherited metabolic disorders can cause multiple movement abnormalities. Dietary modifications, medications, and increasingly specific therapy can improve outcomes in children with movement disorders caused by metabolic disorders. Recognition and characterization of secondary movement disorders in children facilitate management of the abnormal movements and diagnosis, and possible treatment, of an underlying metabolic disorder.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationChristensen, C. K., & Walsh, L. (2018). Movement Disorders and Neurometabolic Diseases. Seminars in Pediatric Neurology. https://doi.org/10.1016/j.spen.2018.02.003en_US
dc.identifier.urihttps://hdl.handle.net/1805/15695
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.spen.2018.02.003en_US
dc.relation.journalSeminars in Pediatric Neurologyen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectneurometabolic diseaseen_US
dc.subjectmovement disordersen_US
dc.subjectmetabolic disordersen_US
dc.titleMovement Disorders and Neurometabolic Diseasesen_US
dc.typeArticleen_US
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