Dystonic Opisthotonus in Kufor-Rakeb Syndrome: Expanding the Phenotypic and Genotypic Spectrum

This syndrome is clinically characterized by juvenile-onset parkinsonism, supranuclear upgaze palsy, cognitive decline, pyramidal signs, visual hallucinations, oculogyric crisis, facial-faucial-finger mini myoclonus and dystonia in various combinations KCI Citation Count: 0

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Bibliographic Details
Published in:Journal of movement disorders 2023, 16(3), , pp.343-346
Main Authors: Gurram, Sandeep, Holla, Vikram V, Kumari, Riyanka, Dhar, Debjyoti, Kamble, Nitish, Yadav, Ravi, Muthusamy, Babylakshmi, Pal, Pramod Kumar
Format: Article
Language:English
Subjects:
Letter to the Editor
신경과학
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Description
Summary:This syndrome is clinically characterized by juvenile-onset parkinsonism, supranuclear upgaze palsy, cognitive decline, pyramidal signs, visual hallucinations, oculogyric crisis, facial-faucial-finger mini myoclonus and dystonia in various combinations KCI Citation Count: 0
ISSN:2005-940X
2093-4939
DOI:10.14802/jmd.23098