Neuromuscular conditions Flashcards

(34 cards)

1
Q

what is cerebral palsy

A

a permanent, non-progressive motor disorder that occurs due to damage to the brain before birth or within 2 years of birth

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2
Q

what is spina bidifa

A

this is the failure of the neural tube to close. It varies in severity

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3
Q

what is muscular dystrophy

A

This is a progressive muscle weakness disease that is genetically inherited

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4
Q

name some types of complex exceptional needs

A
  • learning and mental functions
  • communication problems
  • motor skills
  • self-care
  • hearing and visual difficulties
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5
Q

what is the criteria for a young person to be classified as having complex exceptional needs

A

< 19 yoa, must have at least 4 different impairments and require feeding OR 2 different imprints and require ventilation

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6
Q

what are the causes of cerebral palsy

A
Pre-natal = drugs, smoking, alcohol, rubella, toxaemia, toxoplasmosis
Peri-natal = anoxic injuries, prematurity (most common), infection
Post-natal = infection or head trauma
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7
Q

what are the anatomical classifications of cerebral palsy

A
Monoplegia = one limb affected
Quadraplegia = all limbs affects
Diplegia = lower limbs affected
Hemiplegia = half of the body affected
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8
Q

what are the physiological classifications of cerebral palsy

A
Spastic = characterised by increased muscle tone due to damage within the pyramids or the motor cortex 
Athetoid = non-spastic/fluctuating muscle tone and involuntary movements
Ataxia = caused by damage to the brain stem/cerebellum and result in posture and balance problems
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9
Q

what is meant by monoplegia cerebral palsy

A

one limb affected

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10
Q

what is meant by diplegia cerebral palsy

A

both lower limbs affected

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11
Q

what is meant by quadriplegic cerebral palsy

A

all limbs affected

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12
Q

what is meant by hemiplegic cerebral palsy

A

half of the body affected

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13
Q

what is meant by spastic cerebral palsy

A

characterised by increased and non-fluctuating muscle tone

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14
Q

what is meant by athetoid cerebral palsy

A

fluctuating muscle tone and involuntary movements

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15
Q

what is meant by ataxia cerebral palsy

A

difficulty with posture and balancing

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16
Q

name some clinical signs of cerebral palsy

A
  • speech, hearing and visual problems
  • learning difficulties
  • epilepsy
  • feeding difficulties
  • behavioural problems
17
Q

what is meant by an antalgic gait

A

when the stance phase is relatively short in comparison to the swing phase - this suggests that there is weight bearing pain

18
Q

what is meant by a trandelenberg gait

A

this is when the hip stabiliser muscles have been damaged and the affected hip will dip. the leg of the affected side will swing outwards when walking

19
Q

what are the prerequisites of a normal gait

A
S - stability in stance 
S - no swing
S - save energy
S - step length 
S - safe prepositioning of the foot
20
Q

what is meant by kinematics

A

how the body moves through space - measured in metres

21
Q

what is meant by kinetics

A

the forces that are exerted on the body - measured in newtons

22
Q

what spinal curvature is common in cerebral palsy

23
Q

name some indications of surgery in cerebral palsy

A

to improve sitting, to prevent hip displacement, to prevent respiratory failure

24
Q

in what proportion of those with cerebral palsy does hip displacement occur

25
what is gross motor function and why is it important to determine this in patients
this is a tool that assesses how severe someone cerebral palsy it - it is a scale that determines how well they are walking: Level 1 = walking with no limitations 2 = walking with limitations 3 = walking with a hand held mobility device 4 = using an electronically monitored device 5 = being transported in a manual wheelchair
26
name some things involved in the management of cerebral palsy
- physiotherapy - surgery - muscle relaxants in spastic CP - soft tissue release - bone realignment
27
name the benign form of spina bifida
occulta
28
what can be done during pregnancy to prevent spina bifida
folic acid
29
what is meningocele spina bifida
this is when there is a cyst int he meninges but the nerve roots are intact
30
what is myelomeningocele spina bifida
this is when the nerve roots are exposed or present in the meningeal cyst
31
what are the 2 main types of muscular dystrophy
Duchenne's and Beckers
32
what is Duchenne's muscular dystrophy
this is the most severe form, it is recessive sex linked and children are usually in a wheelchair by the age of 12
33
what is Becker's muscular dystrophy
this is more minor and people are usually in a wheelchair by the age of 30
34
name some clinical signs of muscular dystrophy
shoulders and arms back, tummy sticking out, foot drop, tip toe contractors, thin and weak thighs and thick calfs, poor balance and falls over a lot, learning difficulties