Other neurological conditions Flashcards

1
Q

cerebral palsy

A

neuromuscular disorder
spastic: hypertonia, hyperreflexia
dyskinetic: dystonia, athetosis, chorea
ataxic: cerebellum

monoplegia (one extremity), hemiplegia (half of body), paraplegia (both LEs), quadriplegia (all extremities), diplegia (greater LEs and some UEs)

complications: seizures, intellectual disabilities, contractures, language and cognitive deficits, dysarthria, visual impairments

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2
Q

ataxia

A

lack of coordination while performing voluntary movements
clumsiness, inaccuracy, instability
not smooth, jerky

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3
Q

chorea

A

brief, purposeless, involuntary movements of distal extremities and face

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4
Q

dyskinesias

A

involuntary, non repetitive, stereotyped movements
writhing

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5
Q

dystonia

A

abnormal postures and disruptions of ongoing movement

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6
Q

hemiballismus

A

flinging motions of the extremities

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7
Q

myoclonus

A

brief and rapid contraction of a muscle or group

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8
Q

tremors

A

rhythmic, alternating, oscillatory movements produced by repetitive patterns of muscle contraction and relaxation

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9
Q

parkinson’s

A

hypo kinetic CNS movement disorder
slowly progressive and degenerative pathways in basal ganglia (substantial nigra)
cardial signs: tremor, RIGIDITY, resistive motion, akinesia, festinating gait, falling

stage 1 - 5 (worst)

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10
Q

spina bifida

A

failure of the spinal column to fully form to protect the neural tube

occulta: bony malformation; may not discover until late childhood, red birthmark or patch of hair
cystica: exposed pich of SC and meninges
- with meningocele: protrusion of a sac through the spine with fluid and meninges, but not the spinal cord
- with myelomeningocele: protrusion of a sac through the spine with spinal cord/nerve roots

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11
Q

medical management of spina bifida

A

may not have many symptoms unless severe (such as tethered cord syndrome) and depending on what parts of the spine are involved

may change during growth spurts

during pregnancy, protect the sac from rupturing and from infections that could result in meningitis
shunt may be placed

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12
Q

increase in intracranial pressure

A

could cause intellectual disability
could result in Arnold chiari syndrome (portion of cerebellum and medula oblongata slip down into the foramen magnum to the cervical spinal cord)

if a shunt is blocked or infected (s/s are headache, vomiting, vision/mem problems, inc head size - medical emergency)

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13
Q

muscular dystrophies and atrophies

A

degenerative disorders resulting in mx weakness and decrease in mx mass
hereditary
due to absent mx protein - dystrophin and high creatine kinase

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14
Q

Duchenne’s muscular dystrophy

A

sex linked, recessive, males
enlarged calves
weakness in proximal joints
ambulating with a trendelenburg (waddling) gait, frequent falls
Gower’s sign - use hands to crawl up to thighs to get up off the floor

die around 20s

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15
Q

Becker’s muscular dystrophy

A

variant of duchennes
slower to progress, less severe, less predictable

survival can be in late adulthood if minimal cardiac involvement

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16
Q

arthrogryposis multiplex congenita

A

deformities and joint contractures
may be stable, mild progressive, or improve
heart and spinal defects, torticollis, diaphragm involved
club feet, internal rotation of UEs

17
Q

other types of muscular dystrophy

A
  1. limb-girdle: slow progression, pelvis/shoulder initially affected
  2. fascioscapulohumeral: early adolescence involves face and UEs/scapula, relatively normal life expectancy
  3. spinal: earlier the age of diagnosis, the greater of severity of functional deficits/shorter life expectancy
  4. congenital myasthenia gravis: disorder of transmission of impulses, males
  5. charcot-marie-tooth disease: peripheral nerves, distal leg muscles
  6. myopathies: progress slower and better prognosis, weakness of face/neck/limbs
18
Q

progressive supra nuclear palsy

A

later middle life
loss of voluntary but preserved reflexive eye movements, bradykinesia, rigidity, axial dystonia, pseudo bulbar palsy, dementia

19
Q

huntington’s chorea

A

onset 30-50
choreiform movements and progressive intellectual deterioration
psychiatric disturbance
progressive

20
Q

ALS

A

progressive degeneration of corticospinal tracts (LMN)
onset around 50s
treatment aimed at secondary complications - spasticity, preventing aspirations, contractures, pain

21
Q

Brachial plexus disorder

A

Erb’s palsy: paralysis of C5+6 cervical nerves, partial C7, cannot raise arm, weak elbow flexion, weak scapula, “waiter’s tip”
Klumpke’s palsy: C7+8 + T1 cervical nerve paralysis, no hand/wrist movements, Horner’s syndrome (mitosis, ptosis, sweating)

22
Q

Guillain-Barre syndrome

A

recovery is 2-4 weeks after symptoms
s/s:acute, rapidly progressive polyneuropathy, symmetric mx weakness, mild sensory loss distally, painful extremities, loss of deep tendon reflexes

prognosis: mild/residual neurological deficits, most are ambulatory within 6 mo

23
Q

myasthenia gravis and how is it confirmed

A

autoimmune attacks on neuromuscular receptors
very rare
episodic muscle weakness, usually muscles innervated by cranial nerves
ptosis, diplopia, muscle fatigue after exercise, dysarthria, dysphagia
sensation and deep tendon reflexes intact

**confirmed by response to anticholinesterase drugs

24
Q

multiple sclerosis

A

20-40 yrs
- degeneration of myelin sheath in brain and spinal cord
- CNS lesions, varied neurological symptoms, remissions and exacerbations and/or progressive
deficits in: muscles, sensation, vision (double and acuity), emotion, balance, bladder, cognition, spasticity

25
Q

seizures

A

primary generalized: widespread involvement of both sides of the brain
partial: smaller, localized area (can spread)

26
Q

generalized seizures

A
  1. tonic-clonic/grand mal (starts with aura, then LOC/stiffeneing, then rigidity and relaxation of muscles
  2. myoclonic-akinetic: loss of tone, jerking
  3. petit mal: absence
27
Q

partial focal seizures

A

simple and complex
simple - sudden movement in 1 body part and no change in vital signs

28
Q

lennox-gastaut syndrome

A

severe seizures, intellectual disability, specific EEG pattern
brain disorders

29
Q

landau-kleffner syndrome

A

acquired epileptic aphasic
progressive encephalopathy

30
Q

simple febrile seizures

A

precipitated by a fever
lasts under 10 min
LOS and jerking
do not cause damage/lead to epilepsy

31
Q

status epilepticus

A

prolonged seizures
can sometimes be triggered when medication is stopped abruptly
can be life threatening, medical emergency
remove dangerous objects, place them in sidling, allow seizure to happen, protect head from injury from shaking

32
Q

GBS – residual paresthesia and pain

A

educate the pt on sensory deficits and related ADL adaptive strategies (hot packs are contraindicated, massage will not remedy the hands)

33
Q

other symptoms of MS

A

Early MS adaptation in classroom teaching – high stool to compensate for LE weakness (this is the most common symptom in early stages)

Heat intolerance is a symptom of multiple sclerosis that may be exacerbated in a client who works in a kitchen. Recommending a cooling vest is a solution to decrease this risk of overheating.

34
Q

post concussion syndrome

A

occurs when symptoms of a mild traumatic brain injury last longer than expected after an injury. These symptoms may include headaches, dizziness, and problems with concentration and memory. They can last weeks to months

typically exacerbated by exercise

35
Q

call for medical help with seizure if

A
  • first seizure
  • in water
  • has a second one
  • no consciousness within 5-10 min
  • if it lasts over 5 min
  • diabetic or pregnant