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Cerebellar fits in children with Chiari I malformation
A Pandey1, S Robinson, A R Cohen
1Division of Pediatric Neurological Surgery, Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Insights
Chiari I malformation can cause "cerebellar fits" in children, mimicking epilepsy or syncope. Prompt diagnosis and decompressive surgery effectively resolve these symptoms.
Area of Science:
- Neurology
- Pediatric Neurosurgery
Background:
- Chiari I malformation involves cerebellar tonsil herniation below the foramen magnum.
- Symptomatic Chiari I malformation can present with diverse neurological deficits.
Purpose of the Study:
- To describe children with Chiari I malformation presenting with "cerebellar fits."
- To highlight diagnostic challenges and treatment outcomes for this specific presentation.
Main Methods:
- Retrospective analysis of 47 pediatric patients with symptomatic Chiari I malformation.
- Detailed review of 13 patients presenting with "cerebellar fits," including prior diagnostic evaluations and surgical findings.
- Comparison of tonsillar herniation depth between patients with and without "cerebellar fits."
Main Results:
- Thirteen percent of patients (13/47) presented with "cerebellar fits" (drop attacks, opisthotonos, respiratory compromise).
- These patients were often misdiagnosed, undergoing extensive evaluations for epilepsy or syncope.
- Mean herniation was less in patients with "cerebellar fits" (8.8 mm) compared to those without (13.9 mm).
- Syrinx was rare in this subgroup (1/13).
- All patients with "cerebellar fits" experienced symptom resolution after decompressive surgery.
Conclusions:
- "Cerebellar fits" associated with Chiari I malformation can mimic other serious conditions.
- Failure to consider Chiari I malformation can lead to delayed diagnosis and misdiagnosis.
- Decompressive surgery offers a gratifying resolution for these symptoms.
Object:
The authors describe a series of children with Chiari I malformation who presented with fulminating symptoms of "cerebellar fits" characterized by drop attacks with or without deterioration of consciousness, opisthotonic posturing, and varying degrees of respiratory compromise.
Methods:
A retrospective analysis was undertaken of the medical records of 47 consecutive patients undergoing surgery for symptomatic Chiari I malformations at Rainbow Babies and Children's Hospital. Thirteen (28%) of the 47 patients presented with complaints consistent with cerebellar fits. Before the correct diagnosis was made, nine (69%) of the 13 children had previously undergone evaluation with electroencephalography and/or electrocardicography and Holter monitoring because of suspected cortical epilepsy or cardiogenic syncope. In each of the 13 children magnetic resonance imaging demonstrated pegged cerebellar tonsils herniated below the foramen magnum. A deep indentation or blanched discoloration of the cerebellar tonsils was noted in five (38%) of these 13 patients at the time of surgery. Of patients with symptomatic Chiari I malformations, the mean degree of tonsillar herniation was significantly less for those in whom cerebellar fits occurred than those in whom they were absent (8.8 mm and 13.9 mm, respectively; p = 0.007). In only one of the patients with cerebellar fits was a syrinx present, and this was a small focal lower thoracic collection. Spells resolved after surgery in all patients who presented with cerebellar fits.
Conclusions:
Cerebellar fits may mimic other disorders such as cardiogenic syncope and epileptic seizures. The correct diagnosis may be delayed or the conditions may be misdiagnosed by those who fail to consider Chiari I malformation as a cause of drop attacks, abnormal extensor posturing, and apneic spells in children. The response to decompressive surgery in these patients is gratifying.
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