Chorea-acanthocytosis is a rare autosomal recessive neurodegenerative disorder with a complex clinical presentation comprising of a mixed movement disorder (mostly chorea and dystonia), seizures, neuropathy and myopathy, autonomic features as well as dementia and psychiatric features. Because the differential diagnosis is wide, clinical clues and red flags are important. We report here our observation of characteristic neck and trunk flexion and extension spasms in four cases with advanced chorea-acanthocytosis. © 2010 Movement Disorder Society.
CITATION STYLE
Schneider, S. A., Lang, A. E., Moro, E., Bader, B., Danek, A., & Bhatia, K. P. (2010). Characteristic head drops and axial extension in advanced chorea-acanthocytosis. Movement Disorders, 25(10), 1487–1491. https://doi.org/10.1002/mds.23052
Mendeley helps you to discover research relevant for your work.