Cerebral palsy is a disorder of posture and movement caused by damage to the developing brain. It can occur before, during, or after birth from conditions like infection, lack of oxygen, or head trauma. The main types of cerebral palsy are spastic, dyskinetic, ataxic, and mixed. Symptoms vary depending on the location and severity of brain damage but may include poor muscle control, involuntary movements, weakness, and developmental delays. Treatment focuses on improving mobility, function, and quality of life through therapies, medications, surgery, and equipment. Cerebral palsy has many potential associated problems and complications that also require management.
3. Introduction
• It’s a disorder of Posture and Movement, Occurs
due to damage to immature CNS before, during
or after birth.
• Cerebral palsy is also called as ’Static
Encephalopathy’ because it represents a problem
with brain structure & function.
• Once an area of the brain is damaged, the damage
area does not spread to other areas of brain.
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4. • However, because of its various connections with other areas of
CNS, the lack of functions of other areas & area which is
damaged may interfere with the ability of functions properly.
• Despite its static nature of CNS damage in C.P. clinical features
of disorder may appear to change as child gets older, motor
demands increases with age, motor abilities may not be able to
cope up quickly enough to meet demands.
• Mainly it will interfere with the functional abilities, delayed
motor development, impaired muscle tone, movement patterns.
• When damage occurs before birth or during birth process it is
consider as ‘Congenital Cerebral Palsy’
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5. • Brain damage in early gestational is more likely to produce
moderate to severe motor involvement leads to Quadriplegia,
whereas damage later in gestation may result in primarily
lower extremity motor involvement results into Diplegia.
• If brain is damaged after birth, up to 3 years of age the C.P. is
considered to be Acquired.(Capute & Accardo -1996, ¾
Brain size)
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6. Etiology
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Incidence of C.P. ranges from 1 to 2.5/1000 live
births. It is closely related to prematurity and low
birth weight.
C.P. can have multiple causes, some of which can
be liked to a specific time period.
Generally any condition that causes- Anoxia,
hemorrhage or damage, to the brain can result in
C.P.
8. Prenatal causes
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When the causes of CP is known, roots are related to problems
experienced during intrauterine development, exposure to maternal
infections in early gestational period can increases the risk of CP.
Rh factor is found in RBC (85% populations)
Rh Incompatibility developed when a mother who is Rh(-ve) delivers a
baby Rh (+ve).
Mother becomes sensitive to the baby’s blood & begins to make
antibodies.
9. • The antibodies can develop the ‘kernicterus syndrome’,
characterized by high frequency hearing loss, visual
problems & discoloration of teeth.
• It can be managed by drug- RHoGam, an immunoglobulin
can be given safely after first delivery to neutralize the
consequences.
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10. Other maternal Problems
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The other maternal problems that can place infant
at risk for neurological injuries include- diabetes,
toxemia during pregnancy.
Diabetes can jeopardizes the metabolic deficits
leads to stunted growth of the fetus, delayed tissue
maturations.
Toxemia in pregnancy leads to maternal high blood
pressure, the fetus will be at risk of not receiving
sufficient blood flow and therefore O2 .
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Maldevelopment of brain and other organ system
is commonly seen in C.P. children.
Teratogens is any agent or condition that causes
the defect in fetus,, including radiations, drugs,
toxins, infections, chronic illness.
Genetic disorders and exposure to teratogens
increases the risk of brain malformations.
12. Perinatal Causes
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An infant may experience the asphyxiations results
from anoxia (lack of O2), during labor and delivery.
Prolonged or difficult labor because of breech
presentations(bottom first) or prolapsed umbilical
cord contributes to asphyxia.
Its considered as commonest cause of C.P.
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The other two biggest risk factors for C.P. are prematurity and
low birth weight.
Fetus born with weight 1500g has 30 times high risk of
developing C.P.
A gestational age has less than 37 weeks with low birth weight
are considered as compounding risk for the neurological deficits.
Birth weight <1500g is also a strong risk factor for C.P.
Thus full term baby weighing <1500 grams may be at the risk for
C.P.
14. Postnatal causes
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An infant or toddler may acquire brain
damage secondary to cerebral hemorrhage,
trauma, infections, anoxia
This is very common in road traffic accidents,
shaken baby syndrome, whereas meningitis,
encephalitis, inflammatory diseases
contributes 60% in development of C.P.
15. Types of C.P.
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Distribution
of
involvement
Type of
Abnormal
muscle tone
and Movement
17. All 4 limbs are
involved
Upper extremities
and
lower extremities,
Results from B/L
brain damage
U.L.>>>L.L.
Also has difficulty in
head and trunk
control, less chances
of becoming
ambulated
Trunk control is
also affected to
some extent
Deformities,
contractures
are common.
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18. All 4 limbs
affected
Results from
B/L brain
damage
LL>>> UL,
sometimes
spared
With assistive
devices can be
mobilised
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19. One side of body
affected
Unilateral brain
damage
Usually mobile,
trunk control
affected to lesser
extent
Good prognosis
with moderate to
high IQ
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Hemiplegic
C.P.
20. According to movement differences
Spastic
Dyskinetic Dystonia Athetoid Mixed Ataxic
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21. Spastic
• Spasticity occurs in 75% of all children with CP including
diplegia, hemiplegia, quadriplegia.
• It is found approximately 40% in quadriplegia, 17% diplegia,
21% hemiplegia.
• Spasticity is a complex motor abnormality often described
as hypertonicity in which resistance to passive movements
increases with change of velocity of movement.
• Spasticity, hyperactive stretch reflex, responds to variety of
treatments like BOTOX, Baclofen, Release surgery, Dorsal
Rhizotomy.
• Spasticity causes significant changes such as- longitudinal
growth of muscle fiber, decrease the muscle volume, muscle
unit size, muscle fiber type.
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22. • Furthermore it causes secondary changes like hip
dislocation, scoliosis, knee contractures, excessive torsional
malalignment of femur, tibia, leads to effortful gait patterns,
difficulty in sitting positions, self care activities.
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23. Diplegia
• Most common type of CP.
• White matter infract in the periventricular areas due to
hypoxia leads to diplegic CP.
• Affects bilateral lower limbs which results into difficulty in
gait, balance, co-ordination.
• In standing these patients shows excessive lumbar lordosis,
anterior pelvic tilt, bilateral internal rotations, knee flexion,
in toeing and equinovalgus deformities and foot positions.
• There is slight difference in UE and LE functioning with this
form of CP, UE and trunk is less affected than LE.
• Gait difficulties such as crouched posture, equinus posture
are the greatest concern for these children.
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24. • Bilateral spasticity and weakness in LE increases the energy
expenditures during ambulation, poor co-ordination and
endurance in lower limbs collectively results into restricted
functional mobility within home and in community level.
• These patients often require assistive devices like posterior
walker, crutches, scooter wheelchair for mobility.
• These patients generally have normal cognition but may
have social and emotional difficulties.
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25. Hemiplegia
• It is subtype of C.P in which the child’s upper & lower
extremity on the same side of the body get affected.
• Four main types of lesions results into hemiplegic C.P.
1. Periventricular white matter abnormalities( Most
Common)
2. Cervical- subcortical lesions.
3. Brain malformations.
4. Non-progressive post natal injuries/complications.
• The UE are more affected than LE with more distal
involvement than proximal.
• Spasticity on affected side decreases muscle and bone
growth which further decreases ROM, hence hemiplegic CP
are more tend for contractures and limb length
discrepancies.
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26. • Typical posture seen in hemiplegic CP are as follows-
protracted shoulders. Elbow flexion, wrist flexion, ulnar
deviations, pelvic retractions, internal rotations & flexion,
knee flexion and forefoot planta-flexion.
• These children achieves all Gross and fine motor milestones
but not within typical time frame.
• Two widely used slandered assessments used to evaluate
the UE functioning in children SHUEE and assisting hand
assessment (AHA).
• Cognitive functions is typical in these children, may require
minimal equipments or self care orthotics devices such as
canes.
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27. Quadriplegia
• It is subtype of C.P. in which volitional muscle control of all
Four limbs get severely affected.
• It is often accompanied by neck and trunk regions.
• Periventricular white matter lesions are common findings
seen in most of the neuroimaging findings in children with
quadriplegic CP.
• Lesions affecting the basal ganglia, occipital area often leads
results into visual impairments & seizures.
• Cognition ranges from normal to extremely affected.
• Gross and fine motor skills vary in children from ambulatory
within home with assistive devices to dependent for all.
• Assistive devices may need throughout life span such as-
standers, wheelchairs, bath system, toilet systems,
mechanical elevators.
• Home modifications should be advice for children with
severe disabilities to maximize independence level, mobility,
transitions.
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28. Dyskinetic
• Dyskinesia and movement disorders results into uncontrolled and
involuntary movements which includes athetosis, rigidity, tremors,
dystonia, ballismus, choreoathetosis.
• Deep gray matter lesions often affected majorly, whereas
periventricular white matter lesions may also affect to lessor
extents.
• Athetosis is characterized by involuntary movements that are
slow, writhing; abnormal in timing, direction and usually large
motions at proximal joints.
• Pure athetoid is rare to find in routine clinical practice, often
found with chorea.
• Cortical-basal ganglia- thalamic loop act as sensory sensory and
motor feed forward and feedback mechanism circuit gets affected
in athetosis.
• Individuals with athetosis typically initiate and attempt control of
movement with the jaw and head.
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29. • The cognitive abilities of these children tends to have normal but
ignored due to associated dysarthria.(Normal to above normal
intelligence).
• Tremor, a rhythmic movement of small magnitude, usually of the
smaller joints, rarely occurs as an isolated disorder in CP but
rather in combination with athetosis or ataxia.
• Dystonia is characterized by a slow motion which involves one
limb or the entire body and in which the pattern itself may change
over time, whereas Ballismus is the most rare movement disorder
and involves random motion in large, fast patterns usually of a
single limb.
• Choreoathetosis involves jerky movement, commonly of the digits
and varying in the ROM
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30. Ataxic
• Ataxic CP is primarily a disorder of balance and control in the
timing of coordinated movements along with weakness,
incoordination, a wide-based gait, and a noted tremor; results due
to deficits in the cerebellum and often occurs in combination with
spasticity and athetosis.
• Children with ataxia have difficulty with transference of skills, and
may be benefitted from a specific task-oriented approach to
treatment. E.g. sit stand, stepping, weight transfers.
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31. Assessment
• To understand the nature of atypical movement and motor control
pattern that seen in children with CP, the physical therapist must
understand the importance of motor control against gravity, the
development of postural control, and the musculoskeletal
development in typically developing children.
• The purpose of the assessment in CP is
• To discover the functional abilities and strengths of the child.
• Determine the primary and secondary impairments and discover
the desired functional and participation outcomes of the child and
family.
• The therapist must use an integrated and organized approach by
doing observation of child, his interactions, handling of the child in
order to get an accurate baseline of the child’s functional status.
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• Data Collection
• Date of birth
Date of assessment
Chronologic age/adjusted age
Reason for referral
Relevant medical history
Overview of function (a few sentences)
Family and environmental characteristics
Contextual factors (conditions and restraints on function) Assistive
technology/adaptive equipment
• Examination
• Morphology
Functional skills and the capacity for change Gross motor control
Communications
Fine motor control
Social skills/control of behaviour
Objective test results
Observation of posture and movement Individual system review
related to function Neuromuscular
Musculoskeletal
Sensory
Respiratory
33. • Evaluation
• List client’s competencies
Areas of concern
System impairments
Ineffective posture and movement Functional limitations
• Barriers to participation
• Analyse each level and how they interrelate, creating the
functional limitations of the client
• Analyse the potential for change according to the findings
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