🧠 Cerebral Palsy (CP)


1. Definition

  • Cerebral palsy (CP) is a group of permanent, non-progressive motor disorders caused by abnormal brain development or brain injury occurring during the antenatal, perinatal, or early postnatal period <2 years of age.
  • It affects movement, posture, and coordination, and is often accompanied by sensory, cognitive, and communication impairments.

2. Causes

  • Antenatal (most common):

    • Prematurity
    • Intrauterine infections (e.g., TORCH)
    • Genetic syndromes or brain malformations
    • Placental insufficiency
  • Perinatal:

    • Birth asphyxia
    • Complicated or traumatic delivery
  • Postnatal:

    • Neonatal sepsis or meningitis
    • Intracranial hemorrhage
    • Head injury

3. Risk Factors

  • Premature birth (<32 weeks)
  • Low birth weight (<2.5 kg)
  • Multiple gestation (twins, triplets)
  • Infections during pregnancy
  • Prolonged labor or delivery complications
  • Neonatal jaundice/kernicterus
  • NICU admission, ventilation, or seizures in neonatal period

4. Types

Type Description
Spastic (most common) Hypertonia and hyperreflexia; hemiplegia, diplegia, or quadriplegia
Dyskinetic Involuntary movements (athetosis, dystonia)
Ataxic Poor coordination, balance, and depth perception
Mixed Combination of spasticity and dyskinesia

5. Pathogenesis

  • Injury or abnormal development of the immature brain affects motor control centers such as:
    • Motor cortex
    • Basal ganglia
    • Cerebellum
  • Damage is non-progressive, but the clinical manifestations may evolve with age due to muscle contractures and secondary complications.

6. Clinical Presentation

Symptoms

  • Delayed motor milestones
  • Abnormal muscle tone (stiff or floppy)
  • Poor coordination or unsteady movements
  • Feeding difficulties

Signs

  • Asymmetrical movement patterns
  • Persistent primitive reflexes (e.g., Moro, ATNR)
  • Scissoring of legs, toe-walking
  • Positive Babinski reflex

Physical Examination Findings

  • Hypertonia or hypotonia
  • Abnormal gait
  • Muscle contractures
  • Poor postural control

7. Organ & System Complications

System Complications
Musculoskeletal Contractures, scoliosis, hip dislocation
Neurologic Seizures, intellectual disability
Speech & Swallowing Dysarthria, drooling, aspiration, feeding problems
Vision Strabismus, cortical visual impairment
Hearing Sensorineural hearing loss
GI Constipation, GERD, malnutrition
Respiratory Recurrent aspiration pneumonia
Psychosocial Social isolation, caregiver stress

8. Diagnostic Investigations

Test Purpose
MRI brain Identify structural or acquired lesions
Metabolic/genetic tests If MRI is inconclusive or syndromic features
EEG If seizures are present

9. Other Relevant Investigations

Test Purpose
Hearing and vision screening Detect sensory impairments
Swallow study (VFSS) For suspected aspiration/dysphagia
Orthopedic assessment Contractures, scoliosis, hip monitoring
Speech and developmental assessments Evaluate for therapy needs

10. Treatment

Curative/Definitive

  • No cure, but early intervention and therapy improve function and quality of life

Empirical

  • Anticonvulsants for seizures
  • Antispasmodics (e.g., baclofen, diazepam)

Supportive

  • Multidisciplinary care: PT, OT, speech therapy
  • Orthotics and assistive devices
  • Nutritional support (e.g., NG tube, PEG if needed)
  • Special education and behavioral therapy

Palliative

  • Pain management
  • End-of-life planning in severe cases with complex comorbidities

11. Long-Term Medications Side Effects

Treatment Complication Monitoring Expected Results
Baclofen Drowsiness, hypotonia Clinical monitoring, tone assessment Minimal sedation, effective tone control
Diazepam Sedation, dependence Clinical observation No oversedation
Antiepileptics Liver dysfunction, drowsiness LFTs, therapeutic drug monitoring Normal liver function, therapeutic levels
Botox injections Weakness, injection site pain Functional assessment Focal tone reduction
PEG feeding Infection, dislodgement Site care, nutritional follow-up Adequate nutrition, weight gain

12. Surveillance for the Disease

Domain Frequency What to Monitor
Growth & Nutrition Every 3–6 months Weight, feeding, signs of malnutrition
Musculoskeletal Every 6–12 months Contractures, scoliosis, hip subluxation
Neurology As needed Seizure control, cognitive progress
Developmental Ongoing PT, OT, speech therapy progress
Vision/Hearing Yearly or as needed Strabismus, hearing loss
Swallowing/Breathing As needed VFSS, respiratory assessment
Mental Health As needed Behavior, mood, caregiver stress

13. Malaysia Support Group for Parents

Support Group Description Contact/Link
Cerebral Palsy Malaysia (CPM) Advocacy, therapy, and family support Facebook: @cpmalaysia
NASOM (National Autism Society Malaysia)* Useful if CP coexists with ASD traits nasom.org.my
Hospital-Based Rehab Clinics Available in tertiary centers (HKL, HUSM, Penang GH) Via pediatrics or rehab department referral

*Note: Not all children with CP have autism, but some benefit from overlapping services.