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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Brain,pp. Brain abnormalities in Neuromyelitis Optica. Detailed information Article for general public Svenska Se emitio el diagnostico de encefalopatia en el enfwrmedad de NMO y se trato a la paciente con corticoides e inmunoglobulinas intravenosas, con lo que se produjo mejoria clinica y radiologica. Tolerability and safety of rituximab Mab- Thera.

Treatment enfermexad neuromyelitis optica with rituximab: Neuromyelitis optica Devic’s disease. August 27, Post categories: Oligoclonal banding and CT. Expanding the spectrum of neuromyelitis optica: The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.


Lanzillotti-Buonsanti N, Pini G.

Lancet,pp. Identification of new serum autoantibodies in neuromyelitis optica using protein microarrays. J Neurol Sci,pp. Longitudinal involvement of the spinal cord in a patient with lupus related transverse myelitis.

J Comput Assist Tomogr, 11pp. The prognosis is variable: For all other comments, please send your remarks via contact us. J Natl Med Assoc,pp. Arch Neurol ; Clinical characteristics, course and prognosis of relapsing Devic’s neuromyelitis optica.

Intracerebral injection of neuromyelitis optica immunoglobulin G and human complement produces neuromyelitis optica lesions in mice. Neuromyelitis optica spectrum disorder in a patient with systemic lupus erythematosus and anti-phospholipid antibody syndrome.

Multiple Sclerosis East and West, pp. Cancer Treat Rev, 31pp.

Neuromielitis óptica – Síntomas y causas – Mayo Clinic

Magnetic resonance imaging in isolated non-compressive spinal cord syndromes. The patient was diagnosed as suffering from encephalopathy within the context of NMO and she was treated with intravenous immunoglobulins and corticoids, which resulted in a clinical and radiological improvement.

Los anticuerpos antiacuaporina-4 AQ-4 son un biomarcador especifico de esta entidad y, desde su descubrimiento, se ha ampliado el numero de sintomas y datos radiologicos de la enfermedad y se ha definido el concepto de espectro clinico de NMO. BMJ,pp. Reconocerlas es muy importante para hacer un diagnostico precoz, evitar pruebas complementarias no necesarias e instaurar el tratamiento adecuado.


Clinical, laboratory and outcome profiles in 79 cases. A case of diffuse myelitis associated with optic neuritis.

[Encephalopathy and neuromyelitis optica: the importance of recognising atypical symptoms].

Neuromyelitis optica NMO is a rare condition, characterized by myelitis and optic neuritis, which shares a number of clinical and edvic features with multiple sclerosis MS [ 1 — 3 ]. Jacob A, Bogglid M. Its differentiation is important because the treatment and prognosis differ between these two diseases.

Neurology, 73pp. Arq Neuropsiquiatr, 66pp. J Neurol Neurosurg Psichiatry, 79pp. Optic neuritis and myelitis.

Encefalopatia y neuromielitis optica: The spectrum of neuromyelitis optica. Cancer Treat Rev, 31pp. The distribution of multiple sclerosis in the United Kingdom.

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