wk3- neuro diseases Flashcards

1
Q

what is cerebral palsy

A

motor function disorder

caused by a permanent, non progressive brain defect or UML present from birth or slightly after birth

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2
Q

types of cerebral palsy

A
  1. spastic- most common
    -diplegia, quadplegia, hemiplegia
    cerebral motor cortex lesion
  2. ataxia
    cerebellar lesion
  3. dyskinetic
    basal ganglia lesion
  4. mixed

determined by where the lesion is

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3
Q

lesions on cerebral motor cortex result in what?

A

CMC is responsible for voluntary movements

resulting in
- paralysis and weakness
-voluntary control lost
-spastic cerebral palsy

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4
Q

lesions on basal ganglia result in what

A

muscle movement directed by motor cortex

results in
-disturbance in posture and muscle tone
-tremors/involuntary movements
-dyskinetic cerebral palsy (long, slow, uncontrolled writhing)

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5
Q

lesions of the cerebellum

A

C is in charge of timing and patterns of muscle contraction

results in
-loss of smooth muscle contraction
-clumsy
-ataxic cerebral palsy

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6
Q

clinical features of cerebral palsy

A

-abnormal muscle tone
-loss of selective motor contorl
-impaired coordination
-weakness
-LOPS
-loss of proprioception

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7
Q

what happens in gait for spastic hemiplegia

A
  • increased plantarflexion- weak tib ant and tight posterior calf muscles, this resulting in loss of heel strike (foot drop)

-ankle equinus and RF varus

-excessive knee and hip flexion for foot drop

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8
Q

most common deformity in hemiplagia is

A

equinovalgus

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9
Q

what happens in gait for diplagia

A

-tight hamstrings causing over activity of quads with increased knee flexion

-increased hip flexion and anterior pelvic tilt giving a crouching gait look

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10
Q

what happens in quadriplegia gait

A

-increased plantarflexion (foot drop)
-increased knee flexion during stance
-reduced knee flexion during swing
-increased hip flexion with a forward lean and anterior pelvic tilt

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11
Q

key takeaways from gait in cerebral palsy

A

-instabily in stance
-poor foot clearance in swing
-inadequate heel strike
-inadequate step length
-excessive energy expenditure

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12
Q

typical manifesttions in hip, knee, ankle and foot of cerebral palsy

A

hip- flexed
knee- flexed
ankle- equinas
foot- valgus or varus and toe deformities

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13
Q

treatment options for cerebral palsy - mechanical aids

A
  1. foot orthoses- to stabilise STJ motion
  2. ankle foot orthoses (AFO)- to stabilise STJ, ankle and knee motion
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14
Q

what is spina bifida

A

failure of closure of spinal column causing a defect in the neural tube

occurs early in foetal development

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15
Q

types of spina bifida

A

occulta- absence of small portion of vertebrae which rarely affects nervous system

cystica- lump/cyst formation
-meningocele
-myelomeningocele

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16
Q

meningocele

A

herniation of spinal meninges

17
Q

myelomeningocele

A

severe form

open cyst and exposure of CSF, spinal canal and cord/nerves

18
Q

clinical features of myelomeningocele

A

-flaccid paraparesis/paraplegia, leg weakness
-posterior chain atrophy
-steppage gait, apropulsive, poor ankle plantarflexion control

18
Q

types of CMT

A

type 1- demyelination (onset in teens/twenties)

type 2- axonal degeneration (onset in adult life)

18
Q

what is CMT

A

hereditary motor and sensory neuropathy

autosomal dominant condition

19
Q

patho of CMT

A

nerve conduction dysfunction results in weakness and atropy of the leg muscles and the posterior medial muscles gain advantage leading to lateral ankle instability/cavus foot type

this usually plateaus in adulthood

20
Q

clinical features of CMT

A

-weakness of leg muscles
-lateral ankle instability
-cavus foot type
-muscle wasting focal to anterolateral comp
-glove and stocking sensation loss
-lesser toe contracture

21
Q

treatment for CMT

A

-splinting
-surgical - PT tendon transfer
- orthoses and footwear aid

22
Q

what is duchenne muscular dystrophy

A

hereditary myopathy (progressive muscle atrophy)

23
Q

patho of DMD

A

Muttion at position 21 chromosome (short arm of X) so more common in men

24
Q

clinical features of DMD

A

most appear before age 5

-delayed independent walking
-muscle weakness
-abnormal gait
-falls
-difficulty with stairs
-muscle cramping/spasms

25
Q

gait patterns in DMD

A

waddling gait
lumbar lordosis
gowers sign
psudeohypertrophy of calf muscles (adipose)
toe walking due to proximal weakness

26
Q

prognosis of DMD

A

weelchair by 12 years
death early twenties

important to avoid immobilisation to offset contracture but also not overuse as it can speed up muscle breakdown

27
Q

treatment of DMD

A

-splints
-braces
-orthoses/footwear in youth
-surgery- tendon transfers for ROM
-physiotherapy

28
Q
A
29
Q

What is autism

A

Restricted or hyper focused behaviours along with impaired social interaction

30
Q

Diagnosis checklist for autism

A
  • impaired social interaction/communication
    -preservative motor movements
    -need for routine
    -restricted range of interests/focuses
  • intense or diminished sensitivity to sensory/tatile stimuli
    -developmental regression
31
Q

Clinical features of autism

A

-regression of milestones
-hypotonia
-awkward motor skills
-neurocutaneous abnormalities
-seizures

32
Q

How to run a session with someone with autism

A

-run on time
-remove stimulus like bright lights or loud noises

33
Q

What is idiopathic toe walking

A

Typically seen in children when their gait does not begin with a heel strike

34
Q

What does idiopathic toe walking have a link to

A

Equinas

35
Q

Treatment of idiopathic toe walking

A

Equinas
- splinting
-serial casting series
-BTX-A
-surgery (tendo-Achilles lengthening)

Non Equinas
- FF plate
- raise
- orthoses