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Diseases » Neuromyelitis Optica » Introduction
 

Neuromyelitis Optica

Neuromyelitis Optica: Introduction

Neuromyelitis Optica: A demyelinating disorder associated with transverse myelopathy and optic neuritis. More detailed information about the symptoms, causes, and treatments of Neuromyelitis Optica is available below.

Symptoms of Neuromyelitis Optica

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Home Diagnostic Testing

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Neuromyelitis Optica: Complications

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Disease Topics Related To Neuromyelitis Optica

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Wrongly Diagnosed with Neuromyelitis Optica?

Neuromyelitis Optica: Marketplace Products, Discounts & Offers

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Neuromyelitis Optica: Undiagnosed Conditions

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Neuromyelitis Optica: Research Doctors & Specialists

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Causes of Neuromyelitis Optica

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Read more about causes of Neuromyelitis Optica.

News Archives for Neuromyelitis Optica

Medical news articles related to Neuromyelitis Optica include:

Source: HealthDay News

Evidence Based Medicine Research for Neuromyelitis Optica

Medical research articles related to Neuromyelitis Optica include:

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Videos for Neuromyelitis Optica

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Reseach about Neuromyelitis Optica

Visit our research pages for current research about Neuromyelitis Optica treatments.

Clinical Trials for Neuromyelitis Optica

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Neuromyelitis Optica include:

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User Interactive Forums

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Definitions of Neuromyelitis Optica:

A syndrome characterized by acute OPTIC NEURITIS in combination with acute MYELITIS, TRANSVERSE. Demyelinating and/or necrotizing lesions form in one or both optic nerves and in the spinal cord. The onset of optic neuritis and myelitis may be simultaneous or separated by several months. (J Neurol Neurosurg Psychiatry 1996 Apr;60(4):382-387) - (Source - Diseases Database)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Neuromyelitis Optica as a "rare disease".
Source - Orphanet


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