Neuromuscular conditions Flashcards

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

A

scoliosis

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

A

1/3

25
Q

what is gross motor function and why is it important to determine this in patients

A

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
Q

name some things involved in the management of cerebral palsy

A
  • physiotherapy
  • surgery
  • muscle relaxants in spastic CP
  • soft tissue release
  • bone realignment
27
Q

name the benign form of spina bifida

A

occulta

28
Q

what can be done during pregnancy to prevent spina bifida

A

folic acid

29
Q

what is meningocele spina bifida

A

this is when there is a cyst int he meninges but the nerve roots are intact

30
Q

what is myelomeningocele spina bifida

A

this is when the nerve roots are exposed or present in the meningeal cyst

31
Q

what are the 2 main types of muscular dystrophy

A

Duchenne’s and Beckers

32
Q

what is Duchenne’s muscular dystrophy

A

this is the most severe form, it is recessive sex linked and children are usually in a wheelchair by the age of 12

33
Q

what is Becker’s muscular dystrophy

A

this is more minor and people are usually in a wheelchair by the age of 30

34
Q

name some clinical signs of muscular dystrophy

A

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