Literature DB >> 16799907

[NMO-IgG antibodies in neuromyelitis optica: a report of 2 cases].

L Zuliani1, A López de Munain, J Ruiz Martínez, J Olascoaga, F Graus, A Saiz.   

Abstract

INTRODUCTION: Neuromyelitis optica is an inflammatory demyelination disease that selectively affects optic nerves and spinal cord. Recently it has been described that the NMO-IgG antibodies, are highly specific for the diagnosis, although they are also present in partial forms of the disease. The antigen responsible for this immune response seems to be aquaporin-4 water channel. CLINICAL CASE: We describe the detection in our laboratory of NMO-IgG antibodies in two patients, one of them with a neuromyelitis optica and the other one with a recurrent myelitis and subclinical involvement of the optic nerve.
CONCLUSIONS: By using dual immunostaining, confocal microscopy showed that the antibodies of both patients colocalized with that of an anti-aquaporin-4.

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Year:  2006        PMID: 16799907

Source DB:  PubMed          Journal:  Neurologia        ISSN: 0213-4853            Impact factor:   3.109


  2 in total

1.  Anti-aquaporin-4 antibodies in Devic's neuromyelitis optica: therapeutic implications.

Authors:  Romain Marignier; Pascale Giraudon; Sandra Vukusic; Christian Confavreux; Jérôme Honnorat
Journal:  Ther Adv Neurol Disord       Date:  2010-09       Impact factor: 6.570

2.  Revised diagnostic criteria for neuromyelitis optica (NMO). Application in a series of suspected patients.

Authors:  Albert Saiz; Luigi Zuliani; Yolanda Blanco; Bruno Tavolato; Bruno Giometto; Francesc Graus
Journal:  J Neurol       Date:  2007-04-02       Impact factor: 4.849

  2 in total

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