Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: May 20, 2026

Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients
12:23

Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients

Published on: April 14, 2014

[Neuromyelitis optica in children. Two case reports].

B Tosello1, C Halbert, J Mancini

  • 1Service de neurologie pédiatrique, CHU La Timone, Assistance publique-Hôpitaux de Marseille, 264, rue Saint-Pierre, 13005 Marseille, France. barthelemy.tosello@ap-hm.fr

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|July 14, 2012
PubMed
Summary

Devic neuromyelitis optica (NMO) is an autoimmune disorder distinct from multiple sclerosis, identified by specific aquaporin-4 antibodies. High antibody affinity was observed in a patient without brain symptoms, highlighting NMO

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Prenatal small head circumference: Which biomarkers best predict microcephaly?

Early human development·2026
Same author

Deletion of <i>C2orf34</i>, <i>PREPL</i> and <i>SLC3A1</i> causes atypical hypotonia-cystinuria syndrome.

BMJ case reports·2025
Same author

Pathways to epilepsy surgery in children with tuberous sclerosis complex-associated epilepsy.

Revue neurologique·2024
Same author

Revue d'epidemiologie et de sante publique·2023
Same author

Fulminant acute disseminated encephalomyelitis (ADEM). A difficult diagnosis and yet an absolute emergency.

Revue neurologique·2023
Same author

Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants.

Journal of genetic counseling·2023

Area of Science:

  • Neurology
  • Immunology
  • Neuroinflammation

Background:

  • Devic neuromyelitis optica (NMO) is a CNS inflammatory demyelinating disease characterized by optic neuritis and transverse myelitis.
  • NMO is distinct from multiple sclerosis, with aquaporin-4 (AQP4) antibodies serving as a specific serological marker.
  • Brain lesions on MRI do not exclude NMO, particularly in areas rich in AQP4 channels.

Observation:

  • This report details two cases of NMO associated with anti-AQP4 antibodies.
  • One patient presented without symptomatic brain involvement, yet exhibited high anti-NMO antibody affinity for AQP4.
  • Flow cytometry was utilized to assess antibody affinity in the observed cases.

Findings:

  • The presence of anti-AQP4 antibodies is a key diagnostic marker for NMO.

More Related Videos

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
09:29

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4

Published on: August 21, 2017

Related Experiment Videos

Last Updated: May 20, 2026

Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients
12:23

Dynamic Visual Tests to Identify and Quantify Visual Damage and Repair Following Demyelination in Optic Neuritis Patients

Published on: April 14, 2014

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
09:29

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4

Published on: August 21, 2017

  • High antibody affinity for AQP4 can be present even in the absence of overt brain symptoms.
  • Brain lesion location in NMO can overlap with AQP4-rich areas.
  • Implications:

    • Understanding the role of AQP4 antibodies is crucial for accurate NMO diagnosis and differentiation from MS.
    • High antibody affinity may indicate specific disease mechanisms or prognostic factors in NMO.
    • Effective treatment strategies for NMO, such as rituximab, are vital for patients unresponsive to corticosteroids.