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A clinical and etiologic profile of spastic diplegia
Richard Tang-Wai1, Richard I Webster, Michael I Shevell
1Department of Neurology/Neurosurgery, McGill University, Montreal, Quebec, Canada.
Insights
Identifying the cause of spastic diplegia in children is challenging, with periventricular leukomalacia being a common finding, especially in preterm infants. Many cases remain without a clear etiology.
Area of Science:
- Pediatrics
- Neurology
- Neonatology
Background:
- Spastic diplegia is a common form of cerebral palsy.
- Identifying the etiology is crucial for prognosis and management.
- Periventricular leukomalacia is a known cause, particularly in preterm infants.
Purpose of the Study:
- To determine the clinical and etiologic profile of children diagnosed with spastic diplegia.
- To identify factors associated with specific etiologies, particularly periventricular leukomalacia.
Main Methods:
- Retrospective chart review of 54 children with spastic diplegia over 12 years.
- Clinical factors and etiological investigations were analyzed.
- Univariate and binomial logistic regression analyses were performed.
Main Results:
- Periventricular leukomalacia was diagnosed in 44.4% of children, more common in preterm infants (58.1%).
- Etiology remained unidentified in 46.3% of cases.
- Low birth weight, neonatal resuscitation, and early gestation (<33 weeks) correlated with periventricular leukomalacia.
- Abnormal perinatal history was strongly associated with periventricular leukomalacia in term infants (OR 8.67).
Conclusions:
- Approximately half of children with spastic diplegia have an identifiable etiology.
- Periventricular leukomalacia is a significant factor, linked to prematurity and perinatal complications.
- Further research into unidentified etiologies is warranted.
Abstract:
To identify the clinical and etiologic profile of children with spastic diplegia, the medical records of patients with spastic diplegia in a single practice over a 12-year period were systematically and retrospectively reviewed. Clinical factors and possible etiology based on investigations were identified. Univariate and binomial logistical regression analyses were undertaken to identify factors correlating with an etiologic determination. Chart review identified 54 children with spastic diplegia. There were 31 (57.4%) preterm children and 23 (42.6%) term children. Periventricular leukomalacia was diagnosed in 24 (44.4%) children (26.1% of term children, 58.1% of preterm children). An etiology was not identified in 25 (46.3%) children: 14 (60.9%) term children and 11 (35.5%) preterm children. Periventricular leukomalacia among all children correlated with a birth weight less than 2000 gm (P = 0.037), history of neonatal resuscitation (P = 0.004), and gestation less than 33 weeks (P = 0.001). Factors specifically associated with periventricular leukomalacia in term children were a problematic perinatal history (P = 0.011), a history of neonatal resuscitation (P = 0.011), and a history of neonatal respiratory distress (P = 0.046). Regression analysis revealed a correlation between an abnormal perinatal history and an etiology of periventricular leukomalacia among term children (odds ratio 8.67, 95% confidence interval 2.51-29.97, P = 0.001). Approximately half of all children with spastic diplegia encountered in clinical practice will have an etiology identified.
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