Cerebral Palsy Flashcards

1
Q

Definition

A
  • A group of permanent disorders of movement and posture causing activity limitation
  • Resulting from non-progressive lesions to the developing fetal or infant brain

• Affecting mainly the motor centers; cerebral cortex , cerebellum , and basal ganglia
🌺 If the brain injury occurs after the age of 2 years, it is diagnosed as acquired brain injury.

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2
Q

frequent neurologic associations including:

A

• Mental retardation

Epilepsy
  • Impaired hearing ;deafness
  • Impaired vision
  • Emotional disturbances
  • Behavioral disturbances
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3
Q

Causes

A

🤕 Pre-natal (80%)

  • Antenatal Infections
  • Congenital malformations
  • Fetal asphyxia

🤕 Natal (10%)

  • Birth asphyxia
  • Birth trauma

🤕 Post-natal (10%)

  • VLBW with intracranial hemorrhage
  • Meningitis, encephalitis
  • Metabolic e.g. phenyle ketonuria Hypoglycemia
  • Hyper bilirubinemia Hydrocephalus.
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4
Q

Topographic classification: (distribution of motor defect)

A

1- Monoplegia → Only one limb is affected

2- Hemiplegia → Upper and lower limbs on one side are affected

3- Diplegia → All limbs are affected, the lower more affected than the upper limbs

4- Paraplagia → Only both lower limbs are affected

5- Quadriplegia → All the four limbs are affected

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5
Q

Clinical Types

A
  1. Spastic cerebral palsy
  2. Ataxic cerebral palsy
  3. Extrapyramidal (dyskinetic, asthetoid) cerebral palsy
  4. Atonic cerebral palsy
  5. Mixed cerebral palsy
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6
Q

Spastic cerebral palsy

Criteria

A

• The commonest type

• Pyramidal tract lesion (UMNL) signs:
Hypertonia
Hyper reflexia
Positive Babinski sign
May be clonus

• Persistence of primitive reflexes

• Pesudobulbar palsy p feeding disorder (poor suckling & swallowing),
🗣Hot potato speech
👀squint and speech disorders.

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7
Q

Spastic cerebral palsy types

A
  1. Spastic diplegia: 35%
  2. Spastic hemiplegia: 25%
  3. Spastic quadriplegia: 20%
  4. Spastic monoplegia
  5. Spastic paraplegia
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8
Q

Spastic diplegia: 35%

A
  • Bilateral spasticity of the legs that is greater than in the arms
  • More in premature with periventricular leucomalacia
  • Crawling is commando like rather than four limbed crawling.
  • Lower limbs scissoring (application of a diaper is difficult)
  • With paraspinal muscle involvement, the child may be unable to sit.
  • MRI typically shows scarring and shrinkage in the periventricular white matter with compensatory enlargement of the cerebral ventricles
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9
Q

Spastic hemiplegia: 25%

A

Due to in utero or neonatal stroke

  • Decreased spontaneous movements on the affected side
  • Shows hand preference at a very early age
  • Walking is delayed until 18-24 mo (tiptoe walking); gait is circumdactive
  • Examination of the extremities may show growth arrest, particularly in the hand and thumbnail
  • Upper extremity assumes a flexed posture when the child runs
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10
Q

Spastic quadriplegia: 20%

A
  • More ischemia and infection
  • The most severe type
  • Marked motor impairment of all extremities and the high association with mental retardation and seizures
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11
Q

Ataxic cerebral palsy

Criteria

A
  • Hypotonia and hyporeflexia

* Cerebellar ataxiap incoordination of voluntary movements, nystagmus, staccato speech, intention tremors.

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12
Q

Extrapyramidal (dyskinetic, asthetoid) cerebral palsy

A

😟Commonest causes
• Asphyxia, kernictrus

😗Criteria
• Hypotonia (replaced with time with hypertonia & rigidity)
• Chorio asthetoid movements
. Deafness.

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13
Q

Atonic cerebral palsy

A
  • Profound hypotonia p floppy infant

* Preserved deep tendon reflexes

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14
Q

Diagnosis/ clinical

A

A thorough history and physical examination should rule out a progressive disorder of the CNS, including degenerative diseases, metabolic disorders, spinal cord tumor, or muscular dystrophy

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15
Q

Diagnosis, investigation

A

Value: Exclude progressive brain insults and may detect a cause or association

a. CT & MRI
• May detect the cause e.g. brain malformations and spinal cord lesions
• Rule out brain tumors & degenerative brain disease.
• CT scan may be useful for detecting calcifications associated with congenital infections
b. TORCH screen.
c. Genetic evaluation
d. Metabolic screen.
e. For associations: Test for Hearing, Visual function , EEG for seizures

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16
Q

Conditions that can mimic cerebral palsy

A
  • Spinal cord tumors
  • Channelopathies
  • Sandifer syndrome
  • MECP2 duplication
  • Congenital dopa-responsive disorders
  • Genetic spastic paraplegia
  • Some metabolic conditions (GLUT1 deficiency, glutaric aciduria type 1)
  • Ataxia telangiectasia
17
Q

Treatment

A

1-Multidisciplinary approach
2-Assist the patients with their needs e.x. Walkers,hearing aid
3-Medications
-Anti spastic drugs
-Botox Injection
-Levodopa
4- surgery—> tenotomy, tendon transfer, muscle release