Less common phenotypes of myelin oligodendrocyte glycoprotein antibody-related diseases in children deserve more attention.

doi:10.1038/s41390-024-03058-x

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Less common phenotypes of myelin oligodendrocyte glycoprotein antibody-related diseases in children deserve more attention.

Pediatric research - 1 Aug 2024

Wang Xiao-Yu, Jiang Yan, Wu Peng, Ma Jian-Nan, Yuan Ping, Li Xiu-Juan, Jiang Li

Abstract excerpt

BACKGROUND: To facilitate the identification of less common clinical phenotypes of myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) in children. METHODS: We retrospectively reviewed medical records of 236 patients with MOGAD. The following phenotypes were considered to be typical for MOGAD: ADEM, ON, TM, and NMOSD. Less common onset clinical phenotypes were screened out; their clinical and...

Topics

Humans
Myelin-Oligodendrocyte Glycoprotein
Child
Female
Male
Phenotype
Retrospective Studies
Child, Preschool
Magnetic Resonance Imaging
Adolescent
Infant
Autoantibodies
Seizures
Prognosis

Source

Open in PubMed Open full text

Identifiers

PMID: 38438553
DOI: 10.1038/s41390-024-03058-x
PMCID: PMC11499257

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics