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Updated: Mar 26, 2026

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
Published on: August 21, 2017
Painful tonic spasms and brainstem involvement in a patient with neuromyelitis optica spectrum disorder
Corina Roman-Filip1, Aurelian Ungureanu2, Mihaela Cernuşcă-Miţaru3
1Neurology Department, Academic Emergency Hospital, "Lucian Blaga" University Sibiu, Sibiu, Romania.
Abstract:
Neuromyelitis optica (NMO) is an inflammatory-demyelinating disease of the central nervous system classically characterized by optic neuritis and severe myelitis. New diagnostic criteria defined neuromyelitis optica spectrum disorder as limited forms of NMO or diverse neurologic presentations in the presence of specific antiaquaporin-4 antibodies. We report the case of a 57-year-old woman admitted in our department for recurrent attacks of optic neuritis, tetraparesis with severe painful tonic spasms of the left limbs and brainstem involvement. Painful tonic spasms have been described as movement disorders associated with multiple sclerosis, but a growing number of reports describe them in cases of NMO.
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