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Published on: December 5, 2014
Natural history of postparoxysmal hemiparesis in childhood
Insights
Postparoxysmal hemiparesis (PH) in children often follows seizures and is more common in girls. This condition typically affects children with pre-existing brain structure disturbances, suggesting a link to early developmental issues.
Area of Science:
- Pediatric Neurology
- Neuroscience
- Clinical Pediatrics
Background:
- Postparoxysmal hemiparesis (PH) is a neurological condition observed in children.
- Understanding the natural history and underlying causes of PH is crucial for effective management.
Purpose of the Study:
- To investigate the clinical characteristics and natural history of postparoxysmal hemiparesis in a pediatric cohort.
- To identify potential etiological factors and associated conditions in children with PH.
Main Methods:
- Observational study of 43 children diagnosed with postparoxysmal hemiparesis over a 4-year period.
- Analysis of clinical presentation, preceding seizures, duration and type of hemiparesis, EEG findings, and patient history.
Main Results:
- PH is more prevalent in children than adults, and more common in girls than boys.
- Seizures preceding PH were often unilateral clonic with loss of consciousness; PH lasted 1 hour to 2 weeks, typically deficitary or pseudoflaccid.
- A significant proportion of children had a history of prenatal, perinatal, or postnatal disorders, indicating pre-existing brain disturbances.
Conclusions:
- PH in children often occurs in those with compromised brain structures, suggesting vulnerability.
- The corticospinal tract is likely involved, characterized by slow maturation and late development in affected children.
Abstract:
In a period of 4 years, 43 children with postparoxysmal hemiparesis (PH) were observed. Two of them had tumors, five Sturge-Weber's disease, and 36 were "primary". The natural history of these is as follows: PH appears more frequently in children than in adults, girls more frequently suffer from PH than boys. The seizure which precedes the PH is most frequently unilaterally clonic with loss of consciousness. PH lasts mostly between 1 h and 2 weeks and recedes slowly, the type is mostly of the deficitary or pseudoflaccid, and rarely spastic. EEG changes are, in the majority, focal. Most children with PH have got a positive case history of a prenatal, perinatal or postnatal disorder. It weems therefore that PH appears in children with an already disturbed brain structure. The type of hemiparesis points to a pure lesion of the corticospinal tract, which matures slowly and relatively late.
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