Neuro By Ptdi Flashcards
Pain perception testing
Assesses sharp/dull discrimination
Analgesia
Loss of pain sensitivity (inability to feel pain)
Tone
Resistance of muscle to passive elongation, while the individual is attempting to stay relaxed (residual contraction at rest)
Spasticity
Velocity-dependent resistance to passive elongation
Aneurysm
Weakening of the artery wall causing an abnormal localized dilation of an artery. Aneurysms can burst and create bleeding.
Dysarthria
Motor speech disorder affecting the muscles used to produce speech (e.g., lips, tongue, vocal cords)
Asthenia
Generalized muscle weakness commonly found in cerebellar lesions
Primary-progressive MS (PPMS)
Steady disease progression (no interruptions or distinct episodes)
Bradykinesia
Slowness in movement
Kinesthesia
Ability to sense motion of a joint or limb
Dysphonia
Physical disorder of the mouth, tongue, throat, and/or vocal cords, that makes it difficult for a person to speak
Location of Broca’s area
Left Frontal lobe
Pattern of distribution of weakness seen in ALS
Asymmetrical distribution with distal to proximal progression
Cardinal features of Parkinson’s disease
Tremor (at rest)
Rigidity
Akinesia/bradykinesia
Postural instability
TRAP
Upper Motor Neurons
Motor neurons that originate in the brain (cerebral cortex), brain stem, or spinal cord
Lower Motor Neurons
Motor neurons that originate in the cranial nerve nuclei and motor neurons distal to the anterior horn cells of the spinal cord (e.g., nerve roots and peripheral nerves)
Transient Ischemic Accident (TIA)
Ischemia without tissue death which causes a transient episode of neurological dysfunction
Pseudoexacerbation
Transient worsening of MS symptoms. Episodes lasts < 24
hours.
Dysmetria
Inability to judge length or distance of movements
Freezing gait
Moments where there is a sudden stop in movement with a temporary inability to move
Guillain-Barré Syndrome
An auto-immune disorder causing acute inflammation and demyelination of the cranial nerves’ and peripheral nerves myelin sheaths
Lower motor neuron syndrome
Post-polio syndrome
Poliomyelitis symptoms reappearing after at least 15 years of disease stability in people who had been affected by
Poliomyelitis
Aphasia
Impairment of language (speech or written) affecting comprehension and/or production
Motor dysfunction signs and symptoms seen in MS
Weakness, central fatigue, spasticity, impaired balance and coordination, impaired ambulation and mobility
Lower extremity post-stroke spastisity positions
Hip adduction, Hip extension, Hip internal rotation, Knee extension, Ankle plantarflexion and supination, and Toe flexion
Modified Ashworth Scale Grade 1+
Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
Relapse (exacerbation) time in MS
At least 24 hours
Apraxia
A motor disorder causing difficulty planning and performing tasks or purposeful movements (provided that the request or command is understood and he/she is willing to perform the task)
Vertigo
An illusion of movement (i.e. sensation of moving or the
environment around you is moving when it’s not)
Length of time until symptoms of transient ischemic attack
(TIA) resolve
24 hours or less
Phases of Guillain-Barré Syndrome
- Progressive Deterioration, 2. Plateau, 3. Recovery
Decorticate rigidity posture
Shoulder adduction, Elbow flexion, Wrist flexion, Finger flexion, Leg extension and internal rotation, Ankle plantar flexion
Example of motion assistance AFOs
Posterior leaf spring, Steel dorsiflexion spring assist
Wernicke’s aphasia
Receptive aphasia
A type of aphasia characterized by impaired written and spoken language comprehension (despite fluent speech with normal rate and melody)
Left temporal lobe
Impairments seen in posterior cord syndrome
Loss of proprioception, pressure sense, and vibratory sense below level of lesion
Temperature awareness testing
Assesses the ability to distinguish between hot (warm) or cold stimuli
Dysphagia
Difficulty swallowing
Mofidied Ashworth Scale Grade 1
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the ROM
when the affected part(s) is moved in flexion or extension
Relapsing-remitting MS (RRMS)
Relapses followed by recovery and disease stabilization
Spinal shock
A transient period of areflexia immediately following SCI
Caracterizado por total areflexia ~24hrs
W gradual return of reflexes and then hyperreflexia
Allodynia
Non-noxious stimulus produces pain
Vascular syndromes that may present with homonymous hemianopia
MCA syndrome and PCA syndrome
Wheelchair options for person with C5 ASIA A
Manual wheelchair with propulsion aids for short distances (flat surfaces), Power wheelchair with adapted joystick for community
Barognosis
Ability to evaluate weight of object or disciminate weights of obiect when holding objects
Foot orthosis used for pes planus
Longitudinal arch supports, scaphoid pad
Flat foot
Modifiable risk factors for CVA
Smoking, Physical inactivity, Obesity, Diet, Excessive alcohol use
Festinating gait
Gait disturbance seen commonly in people with Parkinson’s disease which is characterized by narrow base with shortened strides with progressively increasing speed
Modified Ashworth Scale Grade 2
More marked increase in muscle tone through most of the
ROM, but affected parts) easily moved
Wenicke’s aphasia is also referred to as
Receptive aphasia
Sialorrhea
Absence of spontaneous swallowing to clear excess saliva (drooling)
Abulia
An absence of willpower or an inability to act decisively
Graphesthesia
ability to identify writing traced on the skin purely by the sensation of touch
Progressive-relapsing MS (PRMS)
Progressive disease from onset with super imposed acute attacks or relapses that may or may not have recovery
Agnosia
Inability to process/interpret sensory information