Midterm Flashcards

1
Q

disease that causes abnormal protein clumps called plaques and irregular knots called neurofibrillary tangles to form in nerve cells in the brain

A

Alzheimers

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2
Q

what physiological effects does Alzheimer’s have on the brain

A

changes in tissues
atrophy
dilated ventricles
widening grooves
sulci and gyri elevations are narrowed

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3
Q

rare, degenerative, genetic
causes generation of nerve cells characterized by motor disturbances , mental deterioration, abnormal behavior

gene mutation causing neurons in brain to degenerate and die

A

Huntington’s

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4
Q

basal ganglia and cerebral cortex begin to atrophy and ventricles become dilated is in which disease

A

Huntington’s

symptoms not evident till 40’s , can be passed to children

dies within 15-20 years

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5
Q

rapid, jerky motions called chorea

A

Huntington’s

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6
Q

progressive, degenerative neurological disorder that produces a syndrome of abnormal movements (tremors, rigidity)

A

Parkinson’s

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7
Q

dopamine producing neurons in a part of the cerebral cortex called basal nuclei and substantia nigra degenerate and die

A

Parkinson’s

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8
Q

bradykinesia = slow movements
repetitive pin finger rolling motion
mask-like appearance
shuffle gait - parkinsonian gait
stooped over, rigid mms, shuffle gait

A

Parkinson’s

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9
Q

demyelination of neurons in the brain and spinal cord including cranial nerves

A

Multiple sclerosis

loss of/blurred vision
progressive mm weakness
speech and hearing impairments
nerve numbness
poor balance

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10
Q

90% of cases of MS

A

relapsing-remitting

relapses lasting weeks to months w states of remission

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11
Q

amyotrophic lateral sclerosis

A

amyotrophic= atrophy of mm fibers/wasting

lateral sclerosis = hardening of sclerosis of lateral pathways of the spinal cord

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11
Q

stationary blood clot =

A

thrombi

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12
Q

floating blood clot =

A

emboli

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13
Q

what blocks blood vessels in a TIA

A

thrombi and emboli

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14
Q

migraine / vascular headache

A

imbalances in brain chemicals of the trigeminovascular system triggering the release of neuropeptides and serotonin which helps regulate pain via the trigeminal nerve

blood vessels become dilated and inflamed resulting in a headache

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15
Q

CN IX (9)

A

glossopharyngeal nerve = glossophayrngeal neuralgia

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16
Q

common cause of all dystrophies

A

genetic defect in dystrophin gene on the x chromosome

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17
Q

dystrophin has a function in the hippocampus w learning and memory functions

A

“Gowers sign” is when you use chair handles to push up to get out of the chair when seated

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18
Q

which muscular dystrophy affects males only

A

Duchenne’s
Beckers

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19
Q

degenerative joint disease/cartilage degenerates

A

osteoarthritis

*most common
- linked to stress on joints over time
- joint P w crepitus, morning stiffness, Herberden’s nodes on DIPs
- joint mice, bone spurs
- age-related 65 +

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20
Q

autoimmune
abnormal response to synovial cells in the synovium of synovial joints

A

rheumatoid arthritis

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21
Q

symmetrical, polyarticular, sm joints involved is what arthritis

A

RA

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22
Q

initiated by activation of T helper cells that produce cytokines, then activate B cells to produce antibodies

A

RA

destruction causes inflammation of synovial membrane w vasodilation, increased permeability and formation of exudate

23
Q

5 steps of RA

A

synovitis
pannus formation
cartilage erosion
fibrosis
ankylosis

24
boutonniere, swan neck, ulnar drift =
can be seen with rheumatoid arthritis
25
no nodules larger joints affected systemic, polyarticular/ oligoarticular
Juvenile RA
26
autoimmune symmetrical "sausage finger" affects skin as well as joints affects axial and appendicular enthesitis is common
psoriatic arthritis
27
stiffness, swelling, pain triggered by a bacterial infection
reactive arthritis
28
invasion of a single joint space (monoarticular) from bacteria, fungus, virus
septic arthritis
29
disorders characterized by 1. lack of sereum markers 2. HLA B-27 protein 3. inflammation of synovial joints
spondyloarthropathy all involve inflammatory back pain, arthritis of SI joints, and intervertebral joints AS, reactive & psoriatic arthritis & arthritis associated w IBD
30
crystallization of urid acid forming tophi, monosodium urate crystals
gout
31
calcium pyrophosphate dihydrate
pseudogout
32
main cause of headaches
decrease levels of neurochemicals like dopamine and serotonin
33
what is the jump sign associated w
myofascial pain syndrome
34
build up of fat and connective tissues from necrosis that make the mm appear larger
pseudohypertrophy seen in muscular dystrophy
35
characteristics of muscular dystrophy
inherited or genetic mms are the targeted tissue symptoms are related to mm wasting progressive
36
a genetic defect in the dystrophin gene on x chromosome
muscular dystrophy rare genetic disease characterized by the atrophy of skeletal mm's
37
most common muscular dystrophy in children
myotonic dystrophy prolonged mm contractions
38
Males only - severe Onset 3-5 y0, W/C by 12, death by 25
Duchennes dystrophy
39
Second most common dystrophy Onset 5-10 yo Males only Shoulder and hip mm’s affected first Less severe, normal lifespan
Becker's
40
dystrophin affects?
hippocampus w learning and memory functions, short term memory problems
41
union of bone, but unacceptable deformity leading to altered biomechanics
malunion
42
bone does not heal even after the repair process has given up - large gap, bone destruction, poor bone health
non-union
43
bone does not heal within expected time frame
delayed union
44
Congenital anomaly (birth defect) from a neural tube defect, the neural tube eventually becomes the brain and spinal cord in a developing embryo Lack of B9 / folic acid
spina bifida
45
3 types of spina bifida
1.Spina bifida occulta - hidden, mildest, most common, one or more SPs fail to unite leaving an open gap posteriorly 2. Myelomeningocele - most severe, SP’s fail to form at multiple locations 3. Meningocele - meninges herniate
46
Tremors, chorea, athetosis, dystonia, myoclonus, tics
movement abnormalities that all have basal ganglia damage
47
skin rash w symmetric proximal mm weakness that can be painful, feels like DOMS P
dermatomyositis
48
can cause paralysis of the digit and thumb extensor mm’s
Posterior interosseous nerve syndrome
49
compression of superficial branch of radial nerve, sensory only nerve, burning/tingling at dorsolateral aspect of hand, wrist and fingers
Cheiralgia paresthetica
50
Motor disorder caused by brain damage in the fetus or during birth/early childhood Abnormal mm tone, reflexes, motor development/coordination
cerebral palsy
51
Neurotransmitters modulate
reward, risk taking, impulsivity, mood, attention, arousal behaviors
52
weakness in shoulder, “winged scapula” affects serratus anterior
long thoracic nerve entrapment
53
virus causing destruction of motor nerves that is highly contagious - causes paralysis, weakness and difficulty breathing
poliomyelitis virus enters fecal-oral route - infects motor neurons in the anterior horn
54
inflammation of brain w swelling and necrosis
encephalitis
55
inflammation of fluid surrounding meninges - can affect brain/spinal cord caused by viruses - pus formation can lead to encephalitis
meningitis swelling and compression on brain tissue and often brain damage
56
related to imbalances in brain chemicals of the trigeminovascular system triggering release of neuropeptides and serotonin which help regulate pain via trigeminal N
migraine / vascular headache blood vessel become dilated and inflamed resulting in a headache