Related Experiment Video
Updated: Jan 23, 2026

High-throughput Flow Cytometry Cell-based Assay to Detect Antibodies to N-Methyl-D-aspartate Receptor or Dopamine-2 Receptor in Human Serum
Published on: November 23, 2013
Little Children, Bigger Problems: Anti-N-Methyl D-Aspartate Receptor Encephalitis!
Ashwini Prithvi1, Shivan Kesavan1, Arushi Gahlot Saini2
1Pediatric Neurology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, 160012, India.
Insights
Anti-N-methyl D-aspartate receptor (NMDAR) antibody encephalitis can affect young children, presenting with severe neurological symptoms. This case highlights a toddler
Area of Science:
- Neurology
- Immunology
Background:
- Autoimmune encephalitis targeting N-methyl D-aspartate receptors (NMDAR) is a recognized neurological disorder.
- While documented in children, its presentation and treatment response in very young toddlers remain less understood.
Observation:
- An 18-month-old boy experienced seizures, movement disorder, cognitive decline, and behavioral changes.
- Cerebrospinal fluid analysis confirmed the presence of NMDAR antibodies.
Findings:
- The child received standard immunomodulatory treatments including pulse corticosteroids and intravenous immunoglobulin.
- Despite treatment, the patient showed a poor response, and no associated tumor was identified.
Implications:
- This case underscores the occurrence of anti-NMDAR encephalitis in toddlers.
- It suggests a potentially poorer treatment response in this age group, warranting further investigation into age-specific therapeutic strategies.
Abstract:
Anti N-methyl D-aspartate receptor (NMDAR) antibody positive autoimmune encephalitis is a well-described entity both in adults as well as in children. The authors report an 18-mo-old boy who presented with seizures, movement disorder, cognitive impairment, and behavioral disturbances. Anti-NMDAR encephalitis was confirmed by detection of NMDAR antibodies in the cerebrospinal fluid. The patient was administered pulse corticosteroids and intravenous immunoglobulin followed by further immunomodulatory therapy. No tumor was detected on screening. The child remained unresponsive to treatment. The authors wish to highlight the occurrence of anti-NMDAR encephalitis in young toddlers and the poor response to therapy often seen in very young children.
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