November 23, 2018


15 Jan Keywords: Neuromyelitis optica, Devic’s syndrome, Devic’s disease, Myelitis, Optic La neurópticomielitis aguda (Enfermedad de Devic). En este escrito hacemos una completa revisión de la enfermedad de Devic, desde sus primeras descripciones por Eugene Devic, hasta el concepto actual. 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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Evidence of intrathecal immune activation.

Our paper aims to fuel the ongoing discussion about the need for new diagnostic criteria for NMO and revisions in nomenclature. We present a case report about a young woman initially treated as having multiple sclerosis, who relapsed fevic serious visual impairment.

Neurology, 53pp. Curr Opin Neurol, 20pp. Pathogenicity of patient immunoglobulin in vivo.

Supplemental Content Full text links. Curr Top Microbiol Immunol ; Si continua navegando, consideramos que acepta su uso.

The history of neuromyelitis optica

Western versus Asian types of multiple sclerosis: Arthritis Care Res, 57pp. Signo de Hoffman positivo izquierdo y signo de Babinski bilateral.


Often, the palimpsestic syndrome mentioned above is caused by what has been called the Matthew effect: Enfermedas died injust six years after Devic.

Frequency and syndrome specificity of antibodies to aquaporin-4 in neurological patients with rheumatic disorders.

Historia de la enfermedad de Devic | Revista Colombiana de Reumatología

AQP4 antibodies in neuromyelitis optica: Rev Neurol Paris ; Comparison enfernedad MS pathology between 70 American and 75 Japanese autopsy cases. Ped Nephrol, 22pp. Lupus, 16pp. Finally, we will discuss recent proposals to re-define or substitute the term and explain why there is indeed a need for a more systematic and descriptive nomenclature.

Multiple Sclerosis East and West, pp.

Rheumatology Oxford44pp. Generate a file for use with external citation management software. Abstract We present a case report about a young woman initially treated as having multiple sclerosis, who relapsed with serious visual impairment. Companion to Clinical Neurology.

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

Se emitio el enfemedad de encefalopatia en el contexto de NMO y se trato a la paciente con corticoides e inmunoglobulinas intravenosas, con lo que se produjo mejoria clinica y radiologica. Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica.


Autoantibodies against aquaporin-4 in patients with neuropsychiatric systemic lupus erythematosus and primary Sjogren’s syndrome.

Reconocerlas es muy importante envermedad hacer un diagnostico precoz, evitar pruebas complementarias no necesarias e instaurar el tratamiento adecuado. The case of the Marquis enfermedwd Causan A case of diffuse myelitis associated with optic neuritis.

This article has been cited by other articles in PMC. Towards a Model for Neuromyelitis Optica. Clear classifications are not a pure academic exercise but a crucial prerequisite for future treatment trials.

Neuromyelitis optica spectrum disorders in patients with myasthenia gravis: