1 Jan INTRODUCTION: Neuromyelitis optica (NMO), or Devic’s disease, is an La neuromielitis optica (NMO) o enfermedad de Devic es un. Summary. Epidemiology. NMO has a worldwide distribution and estimated prevalence of /, Clinical description. Patients present with acute, often . Download Citation on ResearchGate | Manejo del dolor en un caso de neuromielitis óptica (enfermedad de Devic) | Neuromyelitis optica (NMO) or Devic’s.
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Si continua navegando, consideramos que acepta su uso. A serum autoantibody marker of neuromyelitis optica: Generate a file for use with external citation management software. Nat Clin Pract Enfermedda, 4pp. Arch Neurol, 63pp. Neurology, 58pp. Practical Neurology ; 6: Galetta SL, Bennett J.
J Neurol Neurosurg Psychiatry, 77pp. Lupus, 10pp.
[Encephalopathy and neuromyelitis optica: the importance of recognising atypical symptoms].
Deviic We present a case report about a young woman initially treated as having multiple sclerosis, who relapsed with serious visual impairment. One month later, her general state had declined and was accompanied by symptoms of confusion and blindness. Recurrent transverse myelitis associates with anti-Ro SSA autoantibodies. New onset neuromyelitis optica in young Nigerian woman with possible antiphospholipid syndrome: A clinical comparative study of multiple enfermfdad and neuro- Behcet’s syndrome, Journal of Neurology.
Anto-aguaporin-4 antibody is involved in the pathogenesis of NMO: Neuromyelitis optica with CSF examination mimicking bacterial meningomyelitis.
Brain magnetic resonance imaging deviic in acute relapses of neuromyelitis optica spectrum disorders. Is Devic’s neuromyelitis optica a separate disease?
Orphanet: Enfermedad de Devic
Acute transverse myelitis in multiple sclerosis. Patterns of disease activity in multiple sclerosis: Arthritis Care Res, 57pp. Most patients have relapsing attacks separated by months or years with partial recoverywith usually sequential index episodes of ON enfermedaf myelitis. Neurology, 38pp. Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis.
Pract Neurol, 10pp. Lanzillotti-Buonsanti N, Pini G. Expanding the spectrum of neuromyelitis optica: Optic neuritis and multiple sclerosis.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Pathogenicity of patient immunoglobulin in vivo.
The presence of a long spinal cord lesion during revic attacks of myelitis is not required for diagnosis of Asian OSMS. Signo de Hoffman positivo izquierdo y signo de Babinski bilateral. Summary In this paper we do a complete review of Devic’s disease, from its first descriptions by Eugene Devic, to the current concept, which is considered a neuromyelitis optica NMO.
Jacob A, Bogglid M. Lupus, 16pp. Clinical, laboratory and outcome profiles in 79 cases. J E sp Med,pp.
Anti-aquaporin-4 antibodies in Devic’s neuromyelitis optica: Neurol Sci, 25pp. History of Devic’s disease.
European J Neurol, 17pp. We present the different forms of presentation of NMO as well as clinical and laboratory findings that distinguish this entity from multiple sclerosis, a task that frequently is not easy to perform because of the similarity in clinical presentation. Cancer Treat Rev, 31pp. Arth Rheum, 27pp.