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Neuromyelitis Optica Is a Variant of Multiple Sclerosis
Steven L. Galetta, MD;
Jeffrey Bennett, MD, PhD
Arch Neurol. 2007;64(6):901-903.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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Neuromyelitis optica (NMO) is a controversial entity that has been periodically redefined. Initially, the condition was coined by Devic1 as an acute monophasic process characterized by severe bilateral optic neuritis and myelitis. In 1999, the disorder was defined to include patients with relapsing-remitting disease, and new criteria were proposed that included clinical findings, magnetic resonance imaging (MRI), and spinal fluid pleocytosis.2 The recent detection of antibodies in some patients with NMO has been used to further extend the diagnostic criteria of this entity.3-5 While the recent amendments have attempted further differentiation of patient populations with multiple sclerosis (MS) and NMO, there remain no definitive clinical criteria, laboratory testing, neuroimaging, or histopathologic features that separate these 2 disorders as individual nosologic entities.
CLINICAL CRITERIA
The potential clinical course of patients with NMO is not distinct from other forms of demyelinating disease. Some patients with NMO . . . [Full Text of this Article] LABORATORY TESTING
IMAGING
PATHOLOGIC FEATURES
CONCLUSIONS
AUTHOR INFORMATION
Author Affiliations: Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia (Dr Galetta); and University of Colorado at Denver and the Health Sciences Center, Denver (Dr Bennett).
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