Neuro 3 Clinical App Flashcards

1
Q

hippocampal amnesia

A
bilateral lesions of hippocampi
def in anterograde mem (can't learn new)
def in spared procedural and working mem
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2
Q

korsakoff’s syndrome

A

thiamine def, alcoholism
degen of mammillary bodies, hippocampal complex and dorsomedial thalamic nuc

can’t retain new mem, no short to long mem
hard to understand written material and meaning convos
confabulate (frag mem into ones that didn’t occur)

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3
Q

anosmia

A

loss of smell

from viral infection of mucose, obstruction of nasal passages, congenital, chear of cn1 or tumors of floor ant cranial fossa

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4
Q

phantosmia

A

olf hallucination
smell when no odor present
lesion of ant/medial temporal lobe
hippocampus, amygdala, or medial dorsal thalamic nuc

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5
Q

kluver-bucy syndrome

A

bilat temporal lobe lesions in amygdala

visual agnosia, hyperorality, hypermetamorphosis(intensively explore enviro or overreact to visual stim), placidity (no showing of anger/fear), hyperphagia (eat lots), hypersexuality

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6
Q

uncal herniation

A

Uncus and parahippocampal gyrus over the tentorium cerebelli edge, through tentorial notch

compress: midbrain

dilated pupil, slowly (shows side 90%), abnormal eye movements (cniii)
weak m oppo of dilated pupil
respiration affected/abnormal reflexes

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7
Q

conduction deafness

A

def to obstruction/altered transformation of sound to tympanic mem or through ossicle chain (wax buildup, middle ear infection, stapes)

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8
Q

sensorineural deafness

A

dam to cochlea, cnviii, or cochlear nuc (ipsi deaf)

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9
Q

central deafness

A

dam to central pathways
bc of crossing - NOT DEAF
past the cochlear nucleus it is hard to follow conversions (can’t make out voices from background noise)

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10
Q

aica occlusion

A

monaural hearing loss (ipsi)

ispi facial paralysis and inability to look to the side of the lesion (pontine gaze center - horizontal)

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11
Q

auditory agnosia

A

perceive sound, but can’t identify it

unimodal sensory association cortex bilaterally (primary/secondary auditory cortex)

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12
Q

wernicke’s area lesion

A

w. aphasia, receptive or fluent aphasia
can’t understand/comprehend said or written
alexia, agraphia, can talk but has no meaning
in gen - can’t get/know whats going on, isn’t aware something is wrong

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13
Q

broca’s area lesion

A

b. aphasia, expressive or non-fluent aphasia

loss of ability to speak fluently, written grammer issues, can understand spoken and written lang, know whats going on = depressed

can have mutism (severe)
less severe - limited speech, slow, telegraphic speech (nonessential words omitted)
“no if ans or buts” can start to say but struggle to finish

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14
Q

global aphasia

A

non-fluent
lesion of lateral sulcus
brocas and wernickes (mixed transcortical aphasia)
receptive and expressive deficits, reading and writing impaired

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15
Q

transcortical lesion

A

sensory (sim to wern)- fluent, impaired comprehension and naming, mca-pca border zone
motor (sim to brocas)-nonfluent, aca-mca border zone

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16
Q

gigantism

A

excessive levels of GH before puberty

stim epiphyseal plates

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17
Q

acromegaly

A

gh-secreting pituitary adenoma

increased organ, hand, foot, tongue, coarsening facial feat, insulin resistance, glucose intolerance

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18
Q

graves disease

A

hyperthyroidism
increased levels of of Thyroid stim immunoglobulins stim t3/4 syn
TSH low, TH high

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19
Q

hyperthyroidism

A

hyperexcitiability, hyperreflexia, irritability
increased BMR and heat production, sweat- lose weight
increased HH, RR (SOB), tremor, m weak, goiter
EXOPHTHALMOS
graves/thyroid neoplasm - tsh low
secondary or third disorder - tsh high

treat w PTU, thyroidectomy

20
Q

hypothyroidism

A

bone age is less that chronologic age
babies: mental retardation
adults: slow, impaired mem/decreased mental capacity, drowsiness, lack of effort
decreased bmr, heat production, hr, weight gain, cold, hypoventilation, growth and mental retardation
caused by thyroiditis - tsh high = thyroidectomy
secondary or third disorder - tsh low

21
Q

cretinism

A

mental and growth retardation

hypothyroidism in perinatal period

22
Q

goiter

A

high tsh or ts immunoglobulins

23
Q

thyroidistis

A

hypothyroidism
high tsh, low th
autoimmune, antibodies to peroxidase, decrease t3 and t4

24
Q

addisons disease

A

primary adrenocortical insufficiency
low bg, anorexia/weight loss. n/v, weak, low bp, high k, metabolic acidosis, decreased hair, HYPERPIGAMENTATION
INCREASED ACTH, decreased cortisol

25
Q

cushing syndrome

A

primary adrenal hyperplasia
high bg, m wasting, obesity in trunk, round face, buffalo hump, osteoporosis, straie, virilization and menstral disorders, high bp
low ACTH, high cortisol

26
Q

secondary adrenocortical insufficiency

A

acth low, cortisol low, aldosterone levels norm

27
Q

cushing disease

A

secondary, high cortiosal and acth
excess, increased acth and cortisol (pituatary adenoma)
high bg, m wasting, obesity in trunk, round face, buffalo hump, osteoporosis, straie, virilization and menstral disorders, high bp

28
Q

conn syndrome

A

aldosterone secreting tumor
primary hyperaldosteronism
na resorption, k and h secretion
high bp, low k, metabolic alkalosis, low renin

29
Q

21b hydroxylase def

A

virilzation, early puberty, def of glucocorticoids and mineralcorticoids
increased acth
adrenogenital syndrome and hyperplagsia

30
Q

17a hydroxylase def

A

lack of secondary hair
def in glucocorticoids and androgens, excess mineralcorticoids
high acth

31
Q

secondary hyperparathyroidism

A

chronic hypocalcemia (renal fail or vit d def)
increase PTH and hyperplasia of PT glands
ca blood levels are low or normal

32
Q

severe hypomagnesemia

A

sim to ca on pth except in severe cases
inhibits pth syn/storage/secretion
alcoholism

33
Q

primary hyperparathyroidism

A

caused by PT adenomas
high pth, high ca, low p
stones, bones (resorption), and groans (constipation)
ca-phosphate or oxalate stones

34
Q

hypoparathyroidism

A

from removal of PT or T or autoimmune/congential

low pth, low ca, high p

35
Q

pseudohypoparathyroidism

A

high, pth, low ca, high p
Gs protein in kidney is defective
short stature, neck, obesity, subcutaneous calcification, short metatarsals/metacarpals
albright hereditary osteodystrophy

36
Q

humoral hypercalcemia of malignancy

A

malignant tumors secrete PTH-rp

high ca, low p, PTH low

37
Q

rickets

A

vit d def
not enough ca and p for new bone formation in kids
skeletal deformaties and fail to grow

38
Q

osteomalacia

A

adults
vit d def where new bone fails to mineralize = bending and softening of weight bearing bones
can involve chronic renal failure

39
Q

hashimoto thyroiditis

A

hypothyroidism, primary
high tsh, low th
autoimmune, antibodies to peroxidase, decrease t3 and t4

40
Q

sheehan syndrom

A

necrosis of pituatary postpartum
low tsh, th, lh, fsh
no period or lactation

41
Q

hypocalcemia

A

hyperreflexia, spontaneous m twitch, tingle/numb, (+) Trousseau and Chvostek (twitch of hand w bp cuff)

42
Q

hypercalcemia

A

decrease QT interval, faster heart contraction

hyporeflexic, constipation, anorexic, lack of appetite, coma, lethargic

43
Q

causes of hypopituitarism

A

brain damage, pituitary tumor

44
Q

pheochromocytoma

A
adrenal gland tumor of chromaffin tissue 
increased catecholamines 
	Hypertension
	Orthostatic hypotension
	Headaches 
	Sweating
	Palpitations
	Chest pain
	Flushing
	Anxiety
45
Q

Secondary Hyperaldosteronism

A

o A kidney problem
o Hypersecretion of renin
o Excess renin from juxtaglomerular cells of the kidney

46
Q

pedrin deficiency

A

sensorineural hearing loss
SLC26A4 gene
hypothyroidism with goiter