Dextromethorphan-associated neurotoxicity with cerebellar edema (DANCE) syndrome.
S. Angurana, Sujatha Manjunathan, Renu Suthar, Prasanna Samynathan, Pradeep Babu Uppaluri, Shubham Raj, A. Saini
Clinical Toxicology August 6, 2026 DOI: 10.1080/15563650.2026.2707982 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Case report Peer reviewed |
|---|---|
| Sample size | 2 |
| Population | Two children (aged 3 years and 13 months) admitted to a tertiary care hospital in North India with dextromethorphan-associated neurotoxicity with cerebellar edema syndrome after ingesting dextromethorphan-containing cough syrup |
| Interventions | Supportive treatment intravenous methylprednisolone |
| Key findings | Two young children developed encephalopathy with cerebellar cytotoxic edema after ingesting dextromethorphan-containing cough syrup; both recovered rapidly without residual neurological deficits after supportive treatment and intravenous methylprednisolone. The authors propose that this newly described syndrome should be considered early in the differential diagnosis and that dextromethorphan-containing cough syrups should not be prescribed to younger children. |
Abstract
Introduction: Dextromethorphan-associated neurotoxicity with cerebellar edema syndrome is a recently described clinico-radiological condition resembling pediatric opioid use-associated neurotoxicity with cerebellar edema syndrome.
Methods: To describe two children with dextromethorphan-associated neurotoxicity with cerebellar edema syndrome from a tertiary care hospital in North India. The clinical details were obtained from the medical case records of the children admitted with dextromethorphan-associated neurotoxicity with cerebellar edema syndrome during the month of August and September 2025.
Results: We report two children (3 years and 13 months) who presented with encephalopathy following ingestion of dextromethorphan-containing cough syrup for viral prodrome. Magnetic resonance imaging showed T2/FLAIR hyperintensities in bilateral cerebellar hemispheres with diffusion restriction, suggestive of cytotoxic edema. With supportive treatment and intravenous methylprednisolone, both patients recovered rapidly with no residual neurologic deficits.
Discussion: These two cases highlight the occurrence of dextromethorphan-associated neurotoxicity with cerebellar edema syndrome in young children. Sensitization of healthcare providers about dextromethorphan-associated neurotoxicity with cerebellar edema syndrome, early clinical suspicion, confirmation of diagnosis with neuroimaging, and supportive care, may be associate with good neurological recovery.
Conclusion: Dextromethorphan-associated neurotoxicity with cerebellar edema syndrome is a new clinico-radiological condition that occurs following ingestion of dextromethorphan in young children. Similar to the recently published report and cases presented here, early identification and treatment may be associated with favorable neurological recovery. Therefore, this syndrome should be considered in the differential diagnosis at an early stage. There is a need to increase awareness among healthcare providers to avoid prescribing dextromethorphan-containing cough syrups to younger children.