Cerebral Palsy

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Intro & Causes - Brain's Early Hiccups

  • Cerebral Palsy (CP): Permanent, non-progressive motor disorders.

  • Affects movement, tone, posture. From insult to developing fetal/infant brain.

  • Incidence: ~2-3/1000 live births. Most common childhood motor disability.

  • Etiology (Brain Insult Timing):

    • Prenatal (70-80%):
      • Intrauterine infections (TORCH)
      • Maternal: thyroid, toxins, trauma
      • Congenital malformations
      • Multiple gestation
    • Perinatal (10%):
      • Birth asphyxia (HIE)
      • Prematurity (<32 wks, <1500g), IVH, PVL
      • Birth trauma
    • Postnatal (10%):
      • CNS infections (meningitis, encephalitis)
      • Head trauma (NAI)
      • Kernicterus
      • Near-drowning

Grades of periventricular leukomalacia diagram

⭐ Periventricular Leukomalacia (PVL) is the most common ischemic brain injury in premature infants leading to CP, particularly spastic diplegia.

CP Types - Movement Mayhem Map

Types of Cerebral Palsy and Affected Brain Areas

Cerebral Palsy manifests in several primary forms, categorized by movement disorder and affected brain regions. 📌 Mnemonic: Some Days Are Mixed (Spastic, Dyskinetic, Ataxic, Mixed).

TypeKey AreaDominant Feature(s)
SpasticPyramidal Tract↑ Tone, UMN signs. Subtypes: Hemiplegia, Diplegia (scissor gait), Quadriplegia.
DyskineticBasal GangliaInvoluntary movements: Athetosis (slow, writhing), Chorea (jerky), Dystonia (posturing).
AtaxicCerebellumIncoordination, ↓ tone, wide gait, intention tremor.
MixedMultipleCombination of above, e.g., spastic-dyskinetic.

Signs & Dx - Spotting the Signals

  • Key Indicators (Red Flags):
    • Delayed motor milestones (e.g., no head control by 4 months, not sitting by 9 months).
    • Abnormal muscle tone: spasticity (clasp-knife), hypotonia, dystonia, athetosis.
    • Persistent primitive reflexes (e.g., Moro, ATNR > 6 months).
    • Early asymmetric hand function or preference (< 1 year).
    • Feeding/swallowing difficulties.
  • Diagnostic Approach:
    • Clinical diagnosis: history (perinatal risk factors), neurodevelopmental exam.
    • MRI brain: preferred imaging to identify structural lesions (e.g., PVL, HIE changes).
    • Standardized assessments: HINE, GMFCS (I-V).

⭐ Asymmetric tonic neck reflex (ATNR) persisting beyond 6 months is a strong predictor of CP.

Cerebral Palsy Types and Manifestations

Treatment & Co-issues - Care & Companions

  • Multidisciplinary Team (MDT): CRUCIAL
    • Pediatrician, Neurologist, Orthopedician.
    • Physio (PT), Occupational (OT), Speech-Language Therapist (SLT).
    • Psychologist, Social worker.
  • Spasticity Management:
    • PT: Stretching, ROM exercises.
    • Oral: Baclofen, Diazepam, Tizanidine.
    • Focal: Botulinum Toxin A (BoNT-A) injections.
    • Severe/Generalized: Intrathecal Baclofen (ITB), Selective Dorsal Rhizotomy (SDR).
  • Orthopedic Care:
    • Braces, splints, casting.
    • Surgery: Contractures, deformities (tendon release, osteotomy).
    • Hip surveillance (risk of dislocation).
  • Addressing Co-morbidities:
    • Epilepsy (~40%): Antiepileptics.
    • Pain: Identify source, manage.
    • Feeding difficulties/GERD: Nutritional support, G-tube if severe.
    • Drooling: Glycopyrrolate, Salivary BoNT-A.
    • Sensory: Vision/hearing aids.
    • Cognitive/Behavioral: Early intervention, education support.
    • Sleep disturbances.
  • Family Support & Education: Counseling, respite care.

Multidisciplinary team for child with severe spastic CP

⭐ Regular hip surveillance (X-ray) is vital in non-ambulant CP children (GMFCS IV-V) to detect hip displacement/subluxation early.

High‑Yield Points - ⚡ Biggest Takeaways

  • Cerebral Palsy (CP): non-progressive motor disorder from early brain injury (prenatal/perinatal/postnatal).
  • Spastic CP is most common; presents with UMN signs (hypertonia, hyperreflexia).
  • Major risk factors: prematurity, low birth weight, birth asphyxia, intrauterine infections.
  • Associated co-morbidities: seizures (most common), intellectual disability, visual/hearing issues.
  • Diagnosis is clinical; MRI brain confirms structural lesions, rules out progressive disorders.
  • Management: multidisciplinary team approach (physio, OT, speech), symptomatic treatment (e.g., baclofen).

Practice Questions: Cerebral Palsy

Test your understanding with these related questions

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Flashcards: Cerebral Palsy

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Infantile epileptic spasm occurs as an age-specific seizure disorder, before the age of _____

TAP TO REVEAL ANSWER

Infantile epileptic spasm occurs as an age-specific seizure disorder, before the age of _____

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