Related Experiment Video
Updated: May 30, 2026

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Naïve Adolescents at High Risk for Psychosis
Published on: November 21, 2013
Movement disorder emergencies in childhood
F J Kirkham1, P Haywood, P Kashyape
1Southampton University Hospitals NHS Trust, UK. fk@soton.ac.uk
Insights
This study categorizes acute-onset movement disorders in children into psychogenic, inflammatory/autoimmune, and non-inflammatory groups. Early diagnosis is crucial for potentially treatable inflammatory conditions, though outcomes vary.
Area of Science:
- Pediatric Neurology
- Movement Disorders
- Neuroimmunology
Background:
- Literature on pediatric acute-onset movement disorders is fragmented.
- Understanding the diverse etiologies is essential for effective management.
Observation:
- A prospective cohort of 52 children with acute movement disorders was studied.
- Common disorders included chorea, dystonia, tremor, myoclonus, and Parkinsonism.
- Three main etiological groups were identified: psychogenic, inflammatory/autoimmune, and non-inflammatory.
Findings:
- Psychogenic disorders (12 children) were more common in older females, presenting with tremor and myoclonus.
- Inflammatory/autoimmune disorders (22 children) encompassed conditions like N-methyl-d-aspartate receptor encephalitis and Sydenham chorea.
- Non-inflammatory disorders (18 children) included drug-induced, metabolic, vascular, and secondary movement disorders.
Implications:
- Early diagnosis of treatable inflammatory/autoimmune conditions is critical, despite weak evidence.
- Management strategies vary significantly based on the underlying etiology.
- Variable outcomes highlight the need for further research and improved diagnostic approaches.
Abstract:
The literature on paediatric acute-onset movement disorders is scattered. In a prospective cohort of 52 children (21 male; age range 2mo-15y), the commonest were chorea, dystonia, tremor, myoclonus, and Parkinsonism in descending order of frequency. In this series of mainly previously well children with cryptogenic acute movement disorders, three groups were recognised: (1) Psychogenic disorders (n = 12), typically >10 years of age, more likely to be female and to have tremor and myoclonus (2) Inflammatory or autoimmune disorders (n = 22), including N-methyl-d-aspartate receptor encephalitis, opsoclonus-myoclonus, Sydenham chorea, systemic lupus erythematosus, acute necrotizing encephalopathy (which may be autosomal dominant), and other encephalitides and (3) Non-inflammatory disorders (n = 18), including drug-induced movement disorder, post-pump chorea, metabolic, e.g. glutaric aciduria, and vascular disease, e.g. moyamoya. Other important non-inflammatory movement disorders, typically seen in symptomatic children with underlying aetiologies such as trauma, severe cerebral palsy, epileptic encephalopathy, Down syndrome and Rett syndrome, include dystonic posturing secondary to gastro-oesophageal reflux (Sandifer syndrome) and Paroxysmal Autonomic Instability with Dystonia (PAID) or autonomic 'storming'. Status dystonicus may present in children with known extrapyramidal disorders, such as cerebral palsy or during changes in management e.g. introduction or withdrawal of neuroleptic drugs or failure of intrathecal baclofen infusion; the main risk in terms of mortality is renal failure from rhabdomyolysis. Although the evidence base is weak, as many of the inflammatory/autoimmune conditions are treatable with steroids, immunoglobulin, plasmapheresis, or cyclophosphamide, it is important to make an early diagnosis where possible. Outcome in survivors is variable. Using illustrative case histories, this review draws attention to the practical difficulties in diagnosis and management of this important group of patients.
More Related Videos
Related Concept Videos
Gastrointestinal Motility Disorders
Attention-Deficit/Hyperactivity Disorder
Diagnostic Criteria and Symptoms
To diagnose ADHD, symptoms must manifest before age 12 and be evident across multiple settings.
Conduct Disorder
Disorders of the Nervous Tissue
Homeostatic Imbalances:
Alzheimer's disease manifests as a gradual decline in memory and cognitive abilities, attributed to the buildup of amyloid plaques and neurofibrillary tangles in the brain.
Parkinson's disease arises from the...
Alterations in Muscle Tone ll
Disorders of the Skeletal Muscle
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...

