Intro & Causes - Brain's Early Hiccups
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Cerebral Palsy (CP): Permanent, non-progressive motor disorders.
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Affects movement, tone, posture. From insult to developing fetal/infant brain.
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Incidence: ~2-3/1000 live births. Most common childhood motor disability.
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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
- Prenatal (70-80%):

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

Cerebral Palsy manifests in several primary forms, categorized by movement disorder and affected brain regions. 📌 Mnemonic: Some Days Are Mixed (Spastic, Dyskinetic, Ataxic, Mixed).
| Type | Key Area | Dominant Feature(s) |
|---|---|---|
| Spastic | Pyramidal Tract | ↑ Tone, UMN signs. Subtypes: Hemiplegia, Diplegia (scissor gait), Quadriplegia. |
| Dyskinetic | Basal Ganglia | Involuntary movements: Athetosis (slow, writhing), Chorea (jerky), Dystonia (posturing). |
| Ataxic | Cerebellum | Incoordination, ↓ tone, wide gait, intention tremor. |
| Mixed | Multiple | Combination 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.

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.

⭐ 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).
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