Risk Factors
Prematurity and low birth weight
Perinatal hypoxia or ischaemia
Infections (e.g. TORCH, meningitis, encephalitis)
Intracranial haemorrhage
Multiple gestation
Neonatal jaundice/kernicterus
Maternal thyroid disease, substance use
Aetiology
Antenatal: most common (e.g. genetic, infection, vascular insult)
Perinatal: birth asphyxia, traumatic delivery
Postnatal: sepsis, stroke, head injury
Pathophysiology
Damage to motor cortex, basal ganglia, cerebellum, or white matter tracts
Static injury → abnormal tone, posture, and motor function
Non-progressive but functional abilities may change with time
Diagnosis
Types
Spastic (most common): hypertonia, UMN signs, hemiplegic/diplegic/quadriplegic
Dyskinetic: involuntary movements, fluctuating tone (basal ganglia damage)
Ataxic: impaired coordination, balance (cerebellar damage)
Mixed: combination of features
Clinical diagnosis
Delayed motor milestones
Persistent primitive reflexes
Abnormal tone/posture
Asymmetry in movement or handedness before 18 months
Differential Diagnosis
Muscular dystrophy
Spinal cord lesions
Neurodegenerative conditions
Metabolic disorders
Investigations
MRI brain – assess injury pattern
Metabolic/genetic testing if diagnosis unclear
Management
Multidisciplinary: physiotherapy, occupational therapy, speech therapy
Spasticity management – oral baclofen, botulinum toxin, selective dorsal rhizotomy
Orthopaedic interventions – tendon release, bracing
Nutritional and feeding support
Antiepileptics for associated epilepsy
Educational and psychosocial support
Complications & Prognosis
Epilepsy (30–50%)
Feeding difficulties and malnutrition
Hip dislocation, scoliosis
Cognitive impairment, behavioural issues
Respiratory infections (aspiration risk)
Severity varies – many have normal intellect and mobility, others require lifelong care