1.1 Clinical: Intro to Neuro Flashcards

1
Q

Encephalopathy. what does it affect?

A
  • “disease of the brain” generally in its entirety (both cerebral hemispheres).
  • affects the function or structure of the brain
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2
Q

Huntington Disease

A
  1. genetic encephalopathy
  2. begins at age 30-40
  3. progressive autosomal dominant disease;
  4. personality changes, movement disorder, gait disturbances –> bedridden and death ~ 15 years after symptoms begin
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3
Q

Rett Syndrome: what is it? cause? progression?

A
  1. genetic disorder (Genetic but not inherited) almost exclusive to females: (XX vs. male XY)
  2. progressive symptoms start ~ age 12-18 months: deterioration of memory, movements, coordination, communication, seizures
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4
Q

Frontal lobe

A

organizing, planning, problem solving, behavioral/impulse control, personality

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5
Q

Frontal Cortex

A

personality, problem solving, spontaneity, initiation, judgment, impulse control, social and sexual behavior

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6
Q

Temporal Lobes

A

processing auditory information, comprehension of meaningful speech (mainly left hemispheric); memory, visual object recognition and long term storage of sensory input.

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7
Q

Parietal lobe

A

processing of sensory information of touch (right side of brain affects sensation on left side of body, and vice versa) also, taste, temperature, language processing/integration;

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8
Q

Hemispatial Neglect

A

usually involves the Right Parietal Cortex with neglect usually to the contralateral side.

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9
Q

Apraxia

A

Usually involves the left parietal lobe;

An inability to carry out a task despite understanding the command, having the motor function and the will to do so.

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10
Q

Occipital Lobes

A

Primary visual cortex (visual perception). Also Association areas with other lobes (frontal, parietal and temporal)

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11
Q

Limbic System

A

“primitive” brain; produces emotional/instinctual responses

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12
Q

Hippocampus

A

essential to formation of lasting memories.

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13
Q

Thalamus

A

relays sensory information (vision, hearing taste, touch)

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14
Q

Hypothalamus

A

control center for emotions, organizes behaviors, hormone release

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15
Q

Cerebellum

A

at base of brain; regulates muscular coordination, tone, posture, balance, sensory perception. Has greatest concentration of neurons of any brain structure.

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16
Q

Midbrain

A

upper cranial nerves nuclei, relay station for auditory and visual information, finer motor function (red nucleus, substantia nigra)

17
Q

Brown- Sequard Syndrome:

A
  • Unique spinal cord pathology

- Presentation: motor loss opposite sensory loss

18
Q

temporal lobe: left side

A

perception of words, processing details, memory, auditory learning, complex memories, visual and auditory processing

19
Q

temporal lobe: right side

A

perception of melodies, reading facial expressions, visual learning.

20
Q

temporal lobe: left side

A

perception of words, processing details, memory, auditory learning, complex memories, visual and auditory processing

21
Q

temporal lobe: right side

A

perception of melodies, reading facial expressions, visual learning.

22
Q

parietal lobe dysfunction, generally

A

inability to write, lack of recognition, spatial dysfunction (right/left confusion), difficulties with self perception (hemi-neglect)

23
Q

occipital lobe lesions:

A

Lesions can cause color agnosia, movement agnosia, agraphia. visual disturbances

24
Q

Sensory pathways

A
  1. from the peripheral nerves thru the spinal cord to the thalamus then brain
  2. Pain/temperature (anteriolaeral aka spinothalamic tract) crosses right away in spinal cord
  3. vibration/position/deep touch (dorsal column) crosses higher up (low Medulla).
25
Q

Motor Pathways:

A

Corticobulbar/Corticospinal tracts: Cross in pons (bulbar/facial sensation) or
Cross in low Medulla (limbs and body)

26
Q

pons

A

respiration

27
Q

medulla

A

heart rate, breathing swallowing