Cards (31)

  • neuromotor function
    • somatic nervous system - voluntary movements -> skeletal muscle
    • autonomic nervous system (ANS) - involuntary movements -> visceral functions
    • sympathetic (fight or flight)
    • parasympathetic (rest and digest)
  • neuromotor function alterations
    • muscle tone alterations: dystonia - disorders of muscle tone
    • atonia - absence of muscle tone
    • hypotonia - decreased muscle tone
    • hypertonia - increased muscle tone
  • neuromotor function alterations
    • movement alterations: dyskinesia - abnormal muscle movement
    • akinesia - absence of muscle movement
    • hypokinesia - decreased muscle movement (slowed)
    • hyperkinesia - increased muscle movement (tremors, ticks, gait disturbances or restlessness)
  • neuromotor function alterations
    • complete motor performance alterations: upper motor neuron or lower motor neuron
    • paresis - weakness of muscle motor function (reduced ability to move)
    • paralysis - loss of muscle motor function (inability to move)
  • dystonia - disorders of muscle tone
  • dystonia
    • etiology
    • trauma to motor system components (MVC, sports injuries, falls)
    • decreased perfusion to nerve tissue -> hypoxia and atherosclerosis
    • metabolic disorders
    • diabetes, renal disease (damage to peripheral nerves)
    • drug toxicity or side effects
    • tumors involving nervous system tissue
    • end result -> change in motor input to muscle = impaired action potential and conduction
  • dystonia
    • patterns of dystonia (change in muscle tone)
    • flaccidity -> no resistance to stretch; muscle is paralyzed
    • usual cause: LMN disease (spinal or motor nerves, lower motor neuron disease)
    • spasticity -> lack of reflex control with continuous or intermittent spasm
    • hyperactive reflexes
    • usual cause: UMN disease (upper motor neuron disease) includes the brain
    • rigidity - continuous or intermittently firm muscles (hypertonia state)
  • dystonia
    • spinal cord injury - complete or partial resection of spinal cord
    • primary - mechanical injury itself
    • force-induced
    • acceleration-deceleration (car accidents)
    • rotation with deformation (head or butt twists and tears the spinal cord)
    • compression (force on top of head or butt that compresses cord)
    • penetration (bullet, stabbing)
  • dystonia
    • spinal cord injury
    • secondary (inflammation); (something happens and injury is further extended due to edema)
    • secondary injury: extension of injury due to edema
    • impedes blood flow, causes tissue hypoxia
    • hemorrhagic necrosis (bleeding within area necrosis the tissue)
  • dystonia
    • spinal cord injury
    • complete transection
    • blockage of neurotransmission from UMNs to LMNs results in immediate loss of voluntary movement with paralysis below level of injury
    • quadriplegia (all four limbs)
    • paraplegia (bottom half gone)
    • hemiplegia (left or right side gone due to right or left brain injury, respectively)
    • paralysis of respiratory muscles with higher injury (C3 or HIGHER)
    • anesthesia below level of injury
    • initial loss of reflex activity
  • dystonia
    • spinal cord injury
    • spinal shock- period immediately after traumatic event (complication of spinal cord injury)
    • loss of bladder and bowel control
    • lack of descending inputs from higher centers due to interruption of neural pathways to remainder of CNS
    • absent autonomic reflexes results in vasodilation
    • hypotension
    • loss of temperature control below injury
    • return of reflex activity as spinal shock subsides (7-20 days to resolve)
    • muscle and bladder spasms common stimuli
    • can stimulate autonomic hyper-reflexia
  • dystonia
    • spinal cord injury
    • autonomic dysreflexia (hyper-reflexia)- life threatening excessive, uncontrolled ANS response
    • caused by stimulation of sensory receptors below the level of injury
    • sudden onset of hypertension
    • blurred vision, headache, bradycardia
  • dystonia
    • spinal cord injury
    • incomplete (partial) spinal cord injury
    • symptoms vary depending on the area
  • dystonia
    • spinal cord injury
    • intervertebral disk injury
    • herniation: nucleus pulposus herniates through annulus fibrosus
    • clinical manifestations: depend on area (neck or lumbar spine most common)
    • pain
    • numbness
    • reflexes
  • dyskinesia - abnormal muscle movement
  • dyskinesia
    • hyperkinesia - increased muscle movement (tremors, tics, gait disturbances) = movement is excessive
    • Huntington's Chorea - inherited autosomal dominant disease
    • severe degenerative disorder involving basal ganglia and cerebral cortex
    • associated with excess dopamine activity within the basal ganglia
    • loss of gamma-aminobutyric acid (GABA) in basal ganglia
    • progresses to frontal cerebral atrophy (loss of brain matter)
    • nonrepetitive, irregular, involuntary rapid muscle contractions beginning in face, arms
    • progressive dementia
  • dyskinesia
    • hyperkinesia
    • alcohol withdrawal (delirium tremens: DTs)
    • overactive autonomic nervous system results in tremors, hallucinations, seizures, and increased BP
    • (chronic alcohol depresses nervous system and when that is taken away there is an exaggerated response)
  • dyskinesia
    • hyperkinesia
    • Tourette's syndrome - neurotransmission problem involving limbic system
    • lack of muscle coordination, involuntary movements, vocal abnormality
  • dyskinesia
    • hypokinesia - decreased muscle movement
    • Bell's palsy - facial nerve paralysis (7th cranial nerve) usually following inflammatory condition
    • one sided facial droop, weakness, or paralysis
    • stroke
  • dyskinesia
    • combination
    • cerebral palsy - lesion on or damage to brain during fetal development
    • motor involvement
    • symptoms depend on area of brain damaged
    • spastic CP most common: spastic movements, coordination and gait problems, impaired speech
  • dyskinesia
    • combination
    • Parkinson's Disease - degeneration of neurons that produce and store dopamine (neurotransmitters) with increased amounts of cholinergic activity
    • affects motor system due to low dopamine levels = increased cholinergic activity (excitation)
  • dyskinesia
    • combination
    • Parkinson's disease
    • classic manifestations: tremor at rest
    • rigidity
    • bradykinesia
    • short, shuffled, quick gait
    • voice changes (monotone, soft), loss of smell
    • excessive daytime sleepiness, REM behavior disorder (act of dream)
    • diminished autonomic movements result in mask-like facial expression and infrequent blinking, (excess salivation)
    • orthostatic hypotension, neurogenic bladder, constipation
    • depression/anxiety, compulsive behaviors, hallucinations
    • advanced -> intellectual deterioration and dementia
  • Mononeuropathies: damage to single nerve or nerve group
  • mononeuropathies
    • carpal tunnel syndrome - compression of median nerve
    • etiology: trauma or inflammation (tendon) from repetitive use of hand
    • clinical manifestations: pain, loss of grip, numbness or tingling
    • can be repaired
  • Demyelination disorders
    • polyneuropathies: conduction velocity depends on diameter of axon and whether it is myelinated: channels for ions
  • Demyelination disorders
    • polyneuropathies
    • definition of demyelination disorder:
    • precipitating event (infection, trauma, inflammation)
    • damage causes degeneration of myelin which causes slowing and cessation of neurotransmission
  • Demyelination disorders
    • polyneuropathies
    • multiple sclerosis: autoimmune or genetic (women age 20-40)
    • destruction of myelin and plaque formation in brain and spinal cord (demyelination)
    • inflammation around plaque -> scarring replaces axons affecting motor, sensory, and autonomic nerves
  • Demyelination disorders
    • polyneuropathies
    • Guillain-Barre syndrome - acute, sudden onset
    • progressive inflammation of peripheral and sensory nerves causing myelin damage in ascending fashion
    • demyelination followed by remyelination
  • Demyelination disorders
    • polyneuropathies
    • Amyotrophic lateral sclerosis (Lou Gehrig's disease) (ALS, 40-50 years)
    • NON-inflammatory degeneration of motor neurons in cortex, brain stem, and spinal cord
    • initially muscle weakness and fatigue in one muscle group
    • speech, swallowing issues, drooling, no change in mentation
    • aware, alert, orientated throughout disease progression even in advanced stages
  • Demyelination disorders
    • polyneuropathies
    • multiple sclerosis, Guillain-barre syndrome, and ALS
    • clinical manifestations
    • weakness, gait disturbances, fatigue
    • speech
    • autonomic system
  • Neuromuscular junction disorder
    • myastenia gravis: chronic, progressive disorder of neurotransmission affecting peripheral nerves
    • autoimmune production of autoantibodies (IgG antibody complexes) produced by thymus gland
    • acetylcholine receptor sites blocked at neuromuscular junction
    • clinical manifestations: eye muscles drooping, progressing down the face and proximal muscles