Neuro Flashcards

1
Q

Cells of Nervous System

  • dendritic cells: function
  • microglia: strructure, function
  • oligodendroglia: function, destroyed
  • schwwann cells: function
  • astrocytes: function -> BBB, lactate, glutamate, glycogen, ATP, K
  • satellite cells
  • epednymal cells
A
  • APC of NS
  • scant cytoplasm and irreg nuceli -> become larger with activation; will become multi-nuc giant cells in HIV
  • myelinate mult CNS axons; destroyed in MS
  • myelinate PNS
  • form blood brain barrier, store glycogen, provide lactate, release glutamate, release ATP, control K levels
  • support cell body in PNS
  • produce CSF
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2
Q

Neuron

  • structure
  • synaptophysin
  • space concept
  • time concept
  • function
  • red
A
  • cell body contains large, central nucleus; contain nissl substance (basophilic granules),
  • presynatic vesicles have synaptophysin and used as stain in IHC
  • measures ability of impulse to travel down axon; low = slow, high=fast
  • how quickly neuron voltage returns to baseline when stimulated; smaller = quicker to baseline, quicker it can transmit another AP
  • functional unit of nervous sxs
  • sign of irreversible damage -> can be caused by ischemia or hypoxia
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3
Q

Axonal regeneration

  • what is it
  • part w/o contract
  • pathway
A
  • process of axonal regeneration after axons damaged
  • is destroyed
  • cell body becomes edematous, nuceli moves to periphery, increase in nissl substance -> if neurolemma is intact, growth occurs at rate of 1 mm a day
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4
Q

Brain embryology

  • pro
  • Mes
  • Rhomb
A
  • tel (cerebrum) and di (thal, hypothal, pineal gland)
  • Mesencephalon (mid brain)
  • Met (pons and cerebllum), Mye (medulla)
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5
Q

Brain Embryology

  • fully formed
  • reflexes
  • how to measure
A
  • 8 weeks
  • present so that baby can swallow
  • measure deepest most unobstructed part of womb w/ US; normal 8-18
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6
Q

Potters

  • caused by
  • sxs
A
  • bilateral renal agenesis

- limb deformity, flat face, pulm hypoplasia

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7
Q

Polyhydraminos

  • maternal cause
  • fetal cause
  • riley-day: type mutation, codes, epi, sxs, prognosis
  • werdnig-hoffman
A
  • DM
  • obstruction
  • AR, mutation of IKBKAP gene on chrom 9 -> codes for gene helpful in transcription; ashkenazi jew; auto neuropathy (no tears when crying), poor sucking, recurring vomiting (anti emetics), highly variable BP (keep hydrated w/ high sodium content), inappropriate perception to pain, heat and taste, mentation is normal; 30s
  • AR, mutation of SMN1 gene on chrom 5, spinal-muscle atrophy
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8
Q

BBB

  • made of
  • how to pass
  • areas that do not contain
A
  • tight junctions between endo cells and astrocyte podocytes
  • transcellular movement; limited by fat solubility
  • post pit, pineal gland, median eminence, area postrema (vomiting)
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9
Q

Holoproencephaly

  • what is it
  • when does it noramlly occur
  • assocaited w/
A
  • incomplete division of forebrain into 2 hemis
  • usually divides at 5th week of gestation
  • hartfield syndrome (AD/XLD; holopro, ectrodactyly, cleft lip/palate) and patau (trisomy 13, microthalmia, cleft lip/ palate)
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10
Q

Neural Tube

  • formation
  • notochrod
  • close
  • becomes
  • Sonic hedge hog
  • bone morphogenic protein
  • closure: in head, in trunk
A
  • neural plate is formed, notochord helps to form neural groove then converges forming neural fold -> then pinches off at the neural crest to form neural tube
  • helps in formation of neural plate to neural groove; produces SHH; helps form axial skeleton; becomes nucleus pulposus
  • at 4 weeks, 25 th is anterior neuropore and 27th day is post neuropore
  • brain and SC
  • produced by notochord and helps in dev of ventral axis; also plays role in dev of forebrain and dev of visual fields
  • neural cells migrate, neural tube closes, overlying ectoderm closes vs ectoderm closes, neural tube closes, neural crest cells migrate
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11
Q

Testing for neural tube defects

  • which test
  • when
  • abnormal test
  • AFP: increased caused by, decreased caused by
  • estriol: represents, decreased =
  • hCG: increased caused by
  • anterior fails
  • posterior fails
A
  • triple test, measure hCG, AFP and estriol
  • 16-18 wks
  • fetal US, looking for incorrect dating -> if not then will do amnio
  • increased = neural tube defects, ant abd wall defects (omphalocele -> covered, gastroschisis -> not covered) or mult gestation; decreased = downs -> karyotype
  • reflects fetal and placental function, decreased= placental insuff
  • increased -> mult gestation, hydatdiform mole (complete = w/ egg -> cluster of grapes, partial = 2 sperm) or choriocarcinoma
  • anencephaly or encephalocele
  • spina bifida occulta, meningocele, meningomyelocele
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12
Q

Anencephaly

  • what is it
  • why
  • exposed
  • signified by
  • prognosis
A
  • absence of forebrain
  • failure of cephalic end of neural tube to close
  • brain tissue
  • high AFP in maternal serum
  • death right after birth
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13
Q

Encephalocele

  • what is it
  • why
  • location
  • associated w/
  • other neuro problems
  • tx
A
  • brain and meninges protrude through opening in skull
  • failure of neural tube to close
  • midline -> middle of skull, forehead to noe, occiput of skull
  • craniofacial abnormalities
  • hydrocephalus, spastic qudraplegia, microcephaly, dev delay, visual disorder
  • close defect, remove all non functional tissue and fix craniofacial deformity
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14
Q

CSF

  • how is it made
  • vitamin needed to make it
  • enzyme needed; what other organs need this
  • how does it get backed up
  • function
  • flow
  • MC area of stenosis; caused by
  • diff from plasma
A
  • secreted by ependymal cells in choroid plexus and through blood vessels in ventricular walls
  • vit A -> pseudotumor cerebri; if too much vit A too much CSF will be made
  • carbonic anhydrase -> kidney, RBC, GI, muscle, brain, eye
  • protecttion, buoyancy, prevents ischemia, provides chemical stability
  • choroid plexus in lat ventricles -> foramen of monroe -> 3rd ventricle -> cerebral acqueduct -> 4th ventricle -> lateral foramen of luschka and medial foramen of megendie -> subarachnoid layer -> spinal canal -> dural sinuses -> arachnoid granulations -> back into blood
  • aqueduct; TB and meningitis
  • less bicarb, more, Cl ,acidic pH
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15
Q

Deceleration Injuries

  • coup injuries
  • countercoup injuries
  • dx
  • what happens after concusion; importance
A
  • CSF able to get to frontal bone before brain to try and cushion blow
  • brain hits occipital bone
  • non contrast CT -> new blood will be white
  • increase in CSF to try and decrease further damage; if 2nd injury will increase CSF today and pt could herniate brain stem
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16
Q

Cerebral Perfusion Pressure

  • what is it
  • increase in ICP
A
  • Mean arterial pressure - ICP

- will decrease perfusion -> either decrease ICP or increase BP to increase perfusion to brain

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17
Q

Shaken Baby Syndrome

  • what is it
  • epi
  • signs
  • sxs
  • considered
A
  • abusive head injury -> coup-counter coup injuries
  • younger than 12 mnth
  • retinal hemmorrhages
  • normal to comatose
  • child abuse
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18
Q

Chemoreceptor Trigger Zone

  • also called
  • location
  • stimulation
  • concussion
  • tx
A
  • area postrema
  • 4th ventricle
  • dopamine
  • compresses and will cause N/V
  • dimenhydrinate (h1 blocker -> OTC for motion sickness), prochlorperazine (typical Anti-psych), promethazine (H1 blocker), ondansetron ( serotonin blocker)
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19
Q

Hydrocephalus

  • communicating: what is it; flow; enlargement of; newborns; children; adults
  • non-communicating: what is it, ventricles, newborn caused by, children caused by, adult/elderly caused by
  • normal pressure: what happens, ICP, sequelae, sxs
A
  • due to CSF over production or lack of reabsorption; flow is intact; all ventricles enlarged; newborns -> vessels have not retracted causing increase in CSF; children - failure to reabsorb CSF -> secondary to meningitis; adults - pseduotumor cerebri
  • obstruction to normal CSF flow; some ventricles atrophied and other enlarged; newborn - type 2 arnold chiari, hereditary aqueduct stenosis, toxoplasmosis, children: meningitis/ TB; adults and elderly: CA; irritability, increased head circumference, poor feeding, enlarged ventricles on CT
  • decreased CSF absorption -> increased CSF vol -> ventricular enlargement; no increase in ICP bc of brain atrophy; ventricles push against periventricular pathways disrupted; wacky, wobbly, wet
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20
Q

Syncope

  • what is it
  • auto dyfunction: what is it, sequelae, MCC, vs orthostatic
  • new born
  • elderly
  • shy dragger
A
  • fainting/ passing out
  • increased PS tone and decreased symp tone; poor reaction to drop in BP -> DM, ortho will pass out after delay
  • riley day syndrome -> brady cardia/ sinus pause secondary to pacemaker issue
  • sick sinus syndrome
  • 50-60 yrs old, autonomic problems and parkinson sxs
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21
Q

Ortho hypotension

  • caused by
  • what happens
  • when standing
A
  • hypovolemia so not enough blood to compensate
  • systolic drops 20, diastolic drops 10, HR goes up 10-20 bpm
  • gravity pulls blood down to feet -> less blood to heart -> less blood to baroreceptors -> decrease PS to heart -> increase HR and contractility of heart
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22
Q

Vasovagal syncope

  • what is it
  • pathway
  • how is this triggered
  • pilots
A
  • body over reacts to stimulus
  • decreased venous return -> decreased LV filling -> heart going to squeeze hard to get vol out to have normal perfusion (increase sympathetics) -> so much blood pushed out that it stretched baroreceptor -> heart slows down, heart contractility decreases and vasodilates -> pt passes out
  • valsava, fear
  • when going through high g turns supposed to do valsava to prevent blood from leaving head
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23
Q

Bells palsy

  • what is it
  • caused by
  • sxs
  • types/ localization
A
  • facial nerve inflammation or damage at geniculate ganglion in facial canal
  • herpes, zoster, lyme dx, sarcoid
  • weakness or paralysis of all muscles on one side of face; eyelids will not close -> tear production decreases; saliva will pool and leak out of corner of mouth; complain of numbness but facial sensation is intact
  • lesion is above nucleus outside of facial canal-> spares forehead; lesion is in facial canal and all fibers have joined together -> affects forehead
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24
Q

Muscles of the eye

  • sup oblique
  • inf oblique
  • sup rectus
  • inf recuts
  • lat rectus
  • med rectus
A
  • down and out
  • up and out
  • up
  • down
  • outward
  • inward
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25
Q

Hypoglossal

  • function
  • runs
A
  • tongue moevement

- transverse over internal carotid a

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26
Q

Taste

  • ant 2/3
  • post 1/3
A
  • CN 7 -> facial

- CN 9 -> glossopharyngeal

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27
Q

Brachial plexus

  • spinal levels
  • divided
  • n to subclavius
  • dorsal scapular
  • long thoracic
  • suprascapular
  • pec
  • subscapular
  • thoracodorsal
  • axillary
  • radial
  • musculocutaneous
  • median
  • ulnar
  • prox vs distal damage to n
  • erbs palsy: caused by, causes, sxs, also called
  • Klumpe palsy: caused by, sxs
A
  • 5 roots -> 3 trunks -> 6 divisions -> 3 cords -> 4 branches
  • c 5,6 -> stabilizes shoulder girdle
  • c5; rhomboid (stabilize shoulder girdle) , levator sacpulae ( ADducts scapula)
  • c5, c6, c7; serratus ant (rotates scapula); winged
  • c5,c6; suprapinatus (inital abduction of arm) infraspinatus (rotates arm laterally)
  • C5-T1; pec major (ADduction and medial rotation), pec minor (pull scapular forward and down
  • c5, c6; teres major (medial rotation, ADduction, extension), subscapularis
  • c6-8; lat (arm extension, ADduction, medial rotation)
  • c5,6; teres minor (lat rotation of arm), deltoid (abduction of arm); ant shoulder dislocation, surgical neck fracture
  • c5-t1; ar,/forearm extensors; saturday night palsy (wrist drop), humeral fracture
  • c5-7; arm flexor
  • c6-T1; forearm flexor, pronator; prox damage will give popes blessing
  • c8-T1; adductor pollicis; prox damage will give claw hand
  • if problem is distal cannot extend and problem is proximal cannot flex
  • c5-6 injury -> dystonia; decreased sensation, paralysis of deltoid, bicep, infraspinatus –> flexion of hand and internal rotation; waiters tip
  • c8-t1 lesion; paralysis of hand and horners syndrome
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28
Q

Phrenic nerve

  • from
  • innervates
  • irritation
  • something pushing
  • right path
  • left path
A
  • C 3, 4, 5
  • diaphragm
  • causes hiccups
  • run along ant scalene, over brachiocephalic a, post to subclavian v, crosses anterior to root of lung, leaves thorax through vena cava hiatus in diaphragm
  • passes over pericardium of left ventricle and pierces diaphragm separately
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29
Q

Angular gyrus function

A
  • language,number processing, spatial recognition
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30
Q

limbic lobe function

A
  • process emotion, forms new memories, motivation, olfaction
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31
Q

corpus callosum

  • function
  • wafarin
A
  • connects hemispheres, allows comm

- degeneration of corpus callosum (teratogenic)

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32
Q

caudate nucleus

- location

A
  • lateral to lateral ventricle and sup to thalamus
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33
Q

herniation

  • what is it
  • transtentorial
  • subfalcine
  • tonsillar
  • central
  • transcalvarial
  • upward/transtentorial
A
  • brain passes through opening at base of skull
  • medial temporal lobe herniates through gap between crus cerebri and tentorium -> goes from ant fossa to post fossa; ipsi 3rd n palsy, pupillary dilation
  • cingulate gyrus herniate under the falx cerebri; abnormal posturing and coma
  • cerbellar tonsils displace through foramen magnum and compress medulla; alt LOC, abnormal ext, abnormal breathing patterns -> apnea, circulatory collapse
  • diencephalon and parts of temporal tobe squeezes through notch in tentorium cerebelli -> stretch basilar a -> duret hemm -> fatal
  • brain herniates through fracture or surgical site in skull
  • result of increased pressure in posterior fossa causing upward movement of cerebellum; fixed/ dilated pupil, altered LOC
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34
Q

Broca Area

  • location
  • function
  • aphasia
A
  • frontal lobe in dominant hemi
  • language comprehension, speech-associated gestures, action recognition and production
  • inability to generate speech with continues understand
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35
Q

Frontal Lobe Dementia

  • also known as
  • caused by
A
  • Picks dx
  • Tau protein, TDP43
  • personality changes, behavior changes, language problems, muscle/ motor dusturbances
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36
Q

Alzheimer’s

  • what is it
  • gross brain appearance
  • micro changes
  • angiopathy
  • extended care
  • NT
A
  • slow progressive memory loss
  • atrophied
  • neurofibrillary tangles (intra cellular) and senile plaques (extra cellular) from APP w/ core composed of beta amyloid
  • amyloid deposits in vascular walls and damages media and adventitia of cerebral vessels causing thickening of basal membrane -> stenosis of lumen
  • when pt and family cannot perform functions of daily living
  • decreased Ach in hippocampus and nuc basalis
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37
Q

Parietal lobe

  • dominant side
  • left responsible for
  • destruction left
  • non-dominant
  • right responsible
  • destruction right
A
  • left
  • long term memory and process of sensory info
  • verbal
  • right
  • intellectual processor of sensory, visospatial
  • apraxia (cant plan muscle moving_ and hemineglect
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38
Q

Occipital

  • function
  • brodmann area
A
  • visual processing center

- 17

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39
Q

Temporal

  • role
  • wernicke
  • meyers loop
  • seizure
  • amygdaloid nuc
  • inferior medial occipital-temporal cortex
A
  • primary auditory area
  • in dom hemi -> can say words but they do not make any sense
  • optic radiation -> contralateral homo quadrantanopia
  • smell something bc has olfaction
  • KB syndrome
  • retention of visual memories
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40
Q

Kluver- Bucy Syndrome

  • side
  • HIPHIP
A
  • bilateral
  • hypermetamorphosis (excess/rapid change of idea), increased oral exploratory behavior (put everything in mouth), placditiy (no aggression), hypersex and phagia, impaired memory and psychic blindness (objects in visual field treated inappropriately)
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41
Q

Blood supply of head and neck

  • dual supply to brain
  • internal bifurcation
  • ant cerebral
  • middle cerebral
  • lenticulo striate
  • vertebrals become
  • post cerebral
  • PICA
A
  • internal carotid and vertebral a
  • circle of willis (ant cerebral, middle cerebral)
  • medial portion -> only frontal lobe of cerebrum
  • lateral portion of cerebrum -> frontal, parietal and temporal lobes
  • white matter, thal, basal ganglia; susceptible to chronic HTN and diabetes; lacunar infarcts
  • basilar a -> ends as post cerebral a
  • supply occiput, communicate with ant and middle cerebral forming circle of willis
  • wind backwards behind medulla and goes to underside of cerebellum where it splits to medial (between 2 hemis of cerebllum) and lat (inferior surface of cerebellum)rul
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42
Q

Rule of 4 to brain

  • 4 strx in midline
  • 4 strx on side
  • 4 CN medulla, 4 in pons and 4 above pons
  • 4 motor nuclei midline
A
  • motor pathway (corticospinal tract), medial lemniscus (contralateral loss vibration and proprioception), medial long fasiculus (failure to ADduct ipsi eye to nose and nystag of contra eye as if it look lateral), motor nuc (ipsi loss of CN affected - 3, 4, 6, 12)
  • ## spinocerebellar pathway (ipsi ataxia of arm and leg), spinothalamic pathway (contra pain and temp of arm/ leg), sensory nuc of 5th (ipsi alteration of pain and temp on face), symp pathway (ipsi horner syndrome)
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43
Q

Epidural Trauma

  • artery
  • MCC
  • sxs
  • CT
  • tx
A
  • middle meningeal a
  • fracture of temporal bone
  • lucid interval
  • lens shaped bleed
  • neurosurgery consult for craniotomy
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44
Q

Subdural

  • artery
  • sxs
  • CT
  • caused by
A
  • bridging v
  • low leaks
  • cresecent shaped bleed between dura and arachnoid
  • head injuries, rapid deceleration or acceleration, shaken baby syndrome
45
Q

Subarachnoid

  • MCC
  • sxs
  • imaging
  • systemic dx
A
  • berry aneursym
  • headahce and altered level of conciousness
  • white area in center and stretching into sulci to either side; CT and if neg then LP
  • adult polycystic kidney dx, marfans, ehlers-danlos
46
Q

Cerebral Vasospasm

- sxs

A
  • altered mental status and focal neuro deficits
47
Q

Charcot- Bouchard

  • what is it
  • why
  • sequelae
  • sxs
A
  • pseudoaneursym bc of HTN induced hyaline arteriosclerosis of tiny arterioles of basal ganglia
  • weak wall = increased dilation risk
  • rupture causes hemm in basal ganglia, internal capsule, thal, and pons
  • focal neuro deficits
48
Q

Resurring Hemm Stroke

  • what is it
  • caused by
  • deposition of
  • risk
  • location
A
  • recurring lobar hemm
  • cerebral amyloid angiopathy
  • beta amyloid deposited in areteial wall -> weakens wall -> predisposition of to rupture
  • advanced age
  • cerebral hemi and smaller area of brain parenchyma
49
Q

Intracerebral Hemm

  • what is it
  • location
  • caused by
  • dx
  • tx
A
  • bleeding in brain parenchyma
  • basal ganglia
  • tumor, htn, trauma
  • head ct
  • surgery
50
Q

Diffuse Axonal injury

  • what is it
  • caused by
  • CT shows
  • sxs
A
  • acute stretching, shearing, or tearing of brain tissue
  • serious traumatic incidents
  • CT will show petiechial hemm in tracts of white matter
  • pt will be in coma with swelling of brain + increased ICP
51
Q

Direct Trauma of head

- leads to

A
  • increased ICP, neuronal damage, death
52
Q

Increased ICP

  • signs
  • cushing triad
  • management
  • surgery
A
  • headache, n/v, ocular paresis
  • hypertension, decreased respiration (decreased perfucion to brainstem) and pulse
  • elevate head of bed, hyperventilate pt (causes vasoconstriction of cerebral v), administer mannitol, sedate pt (agitation increases ICP)
  • with midline deviation or evidence of herniation
53
Q

Glasgow coma scale

  • eye
  • verbal
  • motor
  • normal
  • minor
  • mod
  • severe
A
  • spontaneous, speech, pain, none
  • oriented to time, person, place; confused ; ianppropriate words; incomprehensible sounds; no response
  • obeys commands; moves to localize pain; flex to withdraw from pain; abnormal flexion; abnormal extension; none
  • 15
  • greater than 13
  • 9-12
  • lower than 8 -> intubate
54
Q

Thalamus

  • function
  • VPL
  • VPM
  • lateral geniculate
  • medial geniculate
  • ventral anterior
  • anterior nucleus
  • lateral posterior
  • medial vs lateral
A
  • relay station for sensory information
  • receives input from spinothal (pain and temp) and medial lemniscus (position and proprioception
  • input from trigeminal and gustatory pathways
  • from optic nerve to optic radiation to visual cortex
  • from auditory pathway (sup olivary nuc and inferior colliculus of pons) and projects to auditory cortex
  • from basal ganglia
  • memory
  • cognition
  • lower vs upper
55
Q

Hypothal

  • controls (5)
  • hunger vs satiety
  • stress
  • cool
  • warm
A
  • hunger/thirst, auto reg, temp, sex behavior, causes release of hormones stored in ant pit
  • lat nucleus -> anorexia; medial nuc -> hyperphagia
  • will release CRH and stim adrenal to release Epi
  • ant
  • post
56
Q

Basal ganglia

  • function
  • direct pathway
  • indirect pathway
  • caudate nuc: function, dx involved in
  • putamen: dorsal striatum; function
  • globus pallidus: function, parts
  • subthal: function
  • substantia niagra: function, NT, dx
A
  • help reg movement
  • cortex initiates movement -> activates putamen -> inhibits GPI -> thalamus activated -> stimulates cortex -> movement
  • cortex stimulates putamen -> inhibits GPE -> inhibits subthal nuc -> GPI stimulated -> increased inhibition of thal -> cortex inhibited
  • important for learning, memory, and language comprehension; loss of GABA cuases Huntingtontons and plays role in OCD
  • w/ caudate nuc; connected to substantia niagra and globus pallidus to help regulate movement
  • involved in reg of voluntary movement; externa and interna
  • inhibited by globus pallidus externa and when activated will produce glutamate to stimulate globus pallidus interna
  • helps initiate movement, NT is dopamine, loss of dopaminergic fibers results in parkinsons
57
Q

Parkinsons

  • caused by
  • sequelae
  • sx
  • best tx
  • levedopa + capone + carbidopa
  • selegeline
  • amantidine
A
  • loss of dopaminergic fibers from sub nigra to striatum
  • diff initiating and stopping movement
  • pill rolling tremor, bradykinesia, shuffle, mask face, auto dysfunction
  • levodopa/cabidopa (best tx -> save till last)
  • broken down in periphery into 3-OMD or dopamine
  • COMT inhibitors allow for levodopa to be converted to dopamine and carbidpoa allows for it to be converted into dopamine in brain instead or periphery
  • MAO-B that prevent breakdown of dopamine
  • increase release of dopamine from nerve terminals; (anti-viral given for Flu)
58
Q

Multiple system atrophy

  • also called
  • what is it
A
  • shy-draggar
  • multi sxs atrophy with either parkinsons sxs or cerebellar sxs
  • uncontrolled autonomics –> ortho hypotesion, constipation, decreased sweat, tears and saliva production
59
Q

Huntingtons Dx

  • genetics
  • causes
  • sxs
  • manage
  • epi
A
  • CAG (glutamine) repeat on HHT gene on chrom 4
  • loss of GABA neurons from caudate nuc
  • personality changes (flat affet, depression, aggitation, addictive behavior) and choreifrom movement
  • anti-pscyh -> dopamine blocker
  • 30-40 yrs
60
Q

Internal capsule

  • location
  • contains
  • damaged by
A
  • between caudate/ thal and lenticular nuc
  • motor fiber
  • lacunar infarcts
61
Q

Lacunar infarct

  • caused by
  • infarct to subtahl
A
  • chronic HTN or DM that causes hyaline arteriosclerosis

- contralateral hemibalismus

62
Q

Midbrain

  • function
  • basal ganglia in midbrain
  • peri aqueductal grey
  • red nuc
  • CN
A
  • movement, addiction, sleep wake cycle
  • sub niagra
  • pain
  • controlling arm swinging and babies crawling; decorticate and decerebrate posturing
  • 3,4
63
Q

Pons

  • pneumotactic center
  • apneuistic center
  • CN
  • central pontine myelinolysis
A
  • responds to elevated CO2 -> adjusts tidal vol and resp rate
  • responds to lower O2 -> will make you inhale deeper
  • 5-8
  • rapid correction of hyponatremia (with saline high in Na or mannitol) or with alcoholism (causes you to pee out water -> hemoconcentrated -> water leaves cell)
64
Q

Medulla

  • function
  • CN
A
  • controls resp rate and other basic functions

- 9-12

65
Q

cerebellum

  • lobes
  • supplied by
  • functionality divided
  • vermis: location, function, damage
  • intermediate zone: location, function
  • flocculonodul lobe: function, what happens with damage
  • lateral hemi: function, damage
  • Dandy walker syndrome: characteristics, sxs, caused by
  • side of sxs when damaged
A
  • ant, post, flocularnodular (on underside)
  • AICA and PICA
  • medial to lateral
  • midline, responsible for posture and motion of trunk; disrupts whole body movement and fine tuned movement
  • lateral to vermis, reg body movement and proprioception to limbs
  • axial muscle balance and tone, spatial relationships, and ocular reflexes; damage causes truncal dystaxia and loss of visual tracking
  • cerebral cerebellum -> responsible for planning movement and for motor learning; dysmetria
  • 4th ventricular enlargement and no vermis and cyst near base of skull; irritability, vomiting, slow motor dev, enlargement of skull, warfarin use during pregnancy
  • ipsilateral; does not obliterate function of movement but movements will not be well coordinated
66
Q

cerebral palsy

  • what is it
  • spastic CP
  • spastic diplegia
  • spastic hemiplegia
  • spastic quadriplegia
  • dyskinetic syndrome
  • atonic
  • ataxic
A
  • permanent neuro damage caused by accident in utero
  • 80% of all cases; clonus, spastic hypertonia, ext plantar responses and hyperreflexia, impaired fine motor; can be
  • only legs affected -> spastic muscles causes knees to turn inwards and legs cross eachother when walking; midline cortical lesion
  • affects one side of body but arm more affected than leg; single sided cortical lesion
  • affect all 4 limbs, trunk, and face; have intellect diability, vision and hearing problems, speech problems
  • caused by perinatal asphyxia (like UC wrapping around neck and suffocating them); lesion of basal ganglia and thal; hypotonia, decreased movement, suppressed reflexes, lethargy, chorea, dystonia
  • caused by frontal lobe involvement; severe hypotonia, microcephaly, cerebral dysgenesis, profound intellect disability
  • wide based gait, tremor in UE, hard time with rapid movement
67
Q

Spinal Cord

  • sensory comes from
  • motor comes from
  • segments
  • ends at
  • filum terminalis
  • blood supply: spinal a , segmental, radicular, aorta
A
  • dorsal root -> ascend
  • ventral root -> to muscle
  • 31
  • L1-2 w/ conus medullaris and cauda equina
  • part of piamater that attaches to sacrum to anchor SC
  • ant spinal artery -> covers 2/3 of SC; right and left post spinal artery off of vertebral a; ant and post segmental a connect directly with ant and post spinal a for anastamoses; radicular a, thoracic and lumbar branches from aorta help bolster blood supply to SC but do not anastamose
68
Q

Ant spinal artery syndrome

  • what happens
  • sxs
A
  • ASA is blocked and no blood supply to ant 2/3 SC

- bowel and bladder dysfunction, loss pain and temp, paralysis of LE

69
Q

Conus medullaris syndrome

  • what is it
  • main sxs
  • caused by
  • ankle jerk
  • side
  • urinary/ impotence
  • time frame
A
  • lesion at L2
  • flaccid paralysis of rectum
  • disk herniation, tumor, spinal fractures
  • exaggerated
  • bilateral, with UMN and LMN sxs (hyper reflexia with fasiculaitons
  • yes
  • sudden
70
Q

Cauda Equina Syndrome

  • caused by
  • sxs
  • reflexes
A
  • massive IV rupture
  • low back pain radiating to one or both legs, saddle anesthesia, loss of anocutaneous reflex, loss of bwel and bladder function,
  • loss of knee and ankle jerk (s1)
  • gradual and unilateral
  • more radicular pain and less back pain
  • asymm arcreflexia paraplegia
  • no impotence
71
Q

UMN vs LMN

  • originates
  • reflex
  • lesion
A
  • UMN: in motor region of cerebral cortex; LMN: from ant horn to muscle
  • Positive babinski (toe up and other toes fan)
  • UMN: spasticity, weakness, decreased motor control, hyperreflexia; LMN: decreased tone, decreased reflex, decreased strength, fasiculation, flaccid paralysis
72
Q

Pyrimidal tracts

  • corticospinal
  • corticobulbar
A
  • from brain to SC to muscle

- from brain to head and neck

73
Q

Extra Pyramidal tracts

  • rubrospinal
  • reticulospinal
  • olivospinal
  • vestibulospinal
A
  • reg voluntary movement in UE
  • trunk and limb muscle tone
  • reflex movement from proprioception
  • head and eye coordination and maintains balance
74
Q

Corticospinal Tract

  • function
  • how
  • originate
  • lat descend
  • ant descend
  • pathology: ALS, Vit B12 def; seizures
A
  • fine motor activity
  • inhibits flexion/extension
  • pre-central gyrus
  • through internal capsule, cross at medullary pyramids and descend through spinal cord
  • will descend straight down to the spinal cord and cross at ant horns
  • pure motor neuron degeneration; affects CS in dorsal column; atonic
75
Q

Spinothalamic Tract

  • function ant
  • function lat
  • cross in
  • 1st synapse
  • 2nd synapse
  • 3rd synapse
  • syringomyelia
A
  • crude touch and pressure
  • pain and temp
  • spinal cord
  • at dorsal horn
  • at thalamus
  • to parietal lobe
  • formation of fluid filled cavity in center of cord; bilateral loss of pain and temp sensation in cape-like division
76
Q

Syringomyelia

  • what is it
  • location
  • associated w
  • sxs
A
  • central cystic dilation of cervical spinal cord
  • enlarges slowly, damages ant horns and ventral white commisure
  • C8-T1
  • arnold-chiari type 2 malformation
  • chronic loss of UE pain and temp sensation, hand muscle atrophy, kyphoscoliosis, UE weakness and hypOreflexia, LE weakness and hypERreflexia
77
Q

Spinocerebellar Tract

  • function
  • part of
  • damage caused by:
A
  • proprioception
  • golgi tendon and muscle spindle
  • alcohol, friedrich ataxia, ataxia telangiectasia, adrenoleukodystrophy (defective long chain FA causing ataxia, hyperpigmentation, muscle spasticity
78
Q

Dorsal Columns

  • function
  • divisions
  • 1st synapse
  • 2nd synapse
  • 3rd synapse
  • vit B12 def
  • other
A
  • fine touch, pressure, vibration, proprioception
  • Gracilis and Cuneatus
  • at medulla
  • at thalamus
  • at parietal lobe
  • paresthesia, peripheral neuropathy, demyelination of both corticospinal tracts and dorsal column
  • tabes dorsalis and brown sequard
79
Q

Tabes Dorsalis

  • caused by
  • causes
  • other sequelae
  • peri-aqueductal grey
  • test
A
  • syphillis
  • degeneration of dorsal column -> loss of positional (romberg sign), vibratory and pain sensation
  • thoracic aortic aneursym
  • pupils fail to constrict in response to light but constrict normally in response to accomodation (Argyll Robertson pupil)
  • FTA-ABS
80
Q

Motor neuron dx

  • what are they
  • ALS
  • PLS
  • Progressive muscular atrophy
  • Progressive bulbar palsy
  • Pseudobulbar palsy
A
  • group disorder only affect motor neurons
  • progressive
  • ALS UMN and LMN
  • LMN, older than 50, LE,
  • LMN, Dx of exclusion; no spcific test fo dx; better prognosis
  • LMN, diff chewing talking and swallowing
  • UMN; cannot control facial movement (uncontrolled laughing and crying)
81
Q

ALS

  • affects
  • epi
  • starts
  • bulbar findings
  • spreads to
  • UMN
  • LMN
  • problems leading to death
  • MCC of death
  • bowels, cognition
  • prognosis
  • managment
  • genetic link
A
  • UMN and LMN
  • middle age male
  • muscle weakness, fasiculation in the tongue
  • 25% pts
  • any muscle of body
  • demyelination of lateral corticospinal tract w/ spasticity and hyper-reflexia
  • loss neurons in ant horn of SC causes muscle weakness and strophy
  • diff chewing and swallowing (asp pneumonia), weakened diaphragm (will need BiPAP and eventually tracheostomy)
  • resp failure
  • super oxide dismutase 1 gene coding, AD, rapid progression
  • continue to work
  • 90% die in 5 years
  • riluzole : blocks Na channels and inhibits glutamate release
82
Q

ALS

  • affects
  • epi
  • starts
  • bulbar findings
  • spreads to
  • UMN
  • LMN
  • problems leading to death
  • MCC of death
  • bowels, cognition
  • prognosis
  • managment
  • genetic link
A
  • UMN and LMN
  • middle age male
  • muscle weakness, fasiculation in the tongue
  • 25% pts
  • any muscle of body
  • demyelination of lateral corticospinal tract w/ spasticity and hyper-reflexia
  • loss neurons in ant horn of SC causes muscle weakness and strophy
  • diff chewing and swallowing (asp pneumonia), weakened diaphragm (will need BiPAP and eventually tracheostomy)
  • resp failure
  • continue to work
  • 90% die in 5 years
  • riluzole : blocks voltage gated Na channels and inhibits glutamate release
  • super oxide dismutase 1 gene coding, AD, rapid progression
83
Q

Anatomic landmark of SC

  • c3
  • c6
  • t1
  • t3
  • t4
  • t5
A
  • hyoid
  • inferior border of cricoid
  • sternoclavicular joint
  • base of spine of scapula
  • bifurcation of trachea, sternal angle
  • sternum proper
84
Q

Spina bifida

  • what is it
  • associated w/
  • labs
  • occulta: what happens, SC, sxs
  • meningocele: what happens, SC
  • meningomyelocele: what happens; associated w; sxs; prevented w/ ; myeloschisis
A
  • incomplete closure of neural tube or overlying vertebrae
  • folate def
  • increased AFP
  • outer vertebrae fails to close completely, but SC cannot pass through; birthamrk, hair, dimple atop error
  • meninges herniates before the vert arch closes, SC in vert canal
  • meninges and SC herniate; arnold chiari 2; hydrocephalus, paralysis and loss of sensory; adequate folate intake; protrusion of exposed nervous tissue to outsdie env
85
Q

Arnold chiari malformation

  • what is it
  • type 1: can cause
  • type 2: can cause
  • type 3: can cause
  • type 4: can cause
A
  • foramen magnum larger than normal, herniation of cerebellar tonsils
  • syringomyelia
  • symptomatic, hydrocephalus and meningomyocele
  • encaphlocele and spina bifida
  • hypoplasia/ aplasia of cerebellum
86
Q

Guillain- Barre syndrome

  • what is it
  • how
  • good px
  • worse px
  • worst complication
  • starts
  • does not affect
  • sxs
  • CSF
  • management
  • miller fisher syndrome
A
  • ascending weakness paralysis that occurs 2 wks after infection (usually after campylobacter)
  • AI that will attack peripheral N
  • damages myelin
  • damages axon
  • resp failure
  • lega and makes way upward to arms and face
  • eye
  • pain, paresthesia
  • high in protein
  • supportive measure, IV Ig to neutralize antibodies and plasmpaharesis
  • guillan-barre of CN; will have opthalmoplegia, ataxia
87
Q

Diabetes

  • pathogenesis of neuropathy
  • where else can it be deposited
  • mono: somatic, cranial
  • auto poly: GI, cardio, sex, urinary
  • distal symmetric poly neuropathy: distribution, motor, sensory,
A
  • diabetic microangiopathy leads to nerve ischemia and sorbitol (aldo reductase) leads to osmotic nerve injury
  • lens -> cataracts
  • bilateral median N, ulnar N, and common peroneal N; 2, 3, 7
  • delayed gastric emptying; orthohypotension; impotence ; over flow inconctinence and neurogenic bladder
  • alove and stocking appearance; weakness and atrophy; paresthesia, loss pain/ temp/ vibration. position
88
Q

Myasthenia Gravis

  • what is it
  • epi
  • dx
  • tx
  • associated w/
A
  • AI attack against Ach receptor
  • middle aged women w/ ptosis
  • anti-ach antibody test; edrophonium test
  • neostigmine/pyridostigmine -> long acting Ach esterase inhibitor
  • chest CT to look for thymoma
89
Q

Lambert Eaton Syndrome

  • Antibodies against
  • associated w
  • muscle affected
  • dx
  • tx
  • diff from MG: location of start, mech, activity, nerve stimulation
A
  • voltage gated Ca in presynaptic N -> cant get ACH out of vessicles
  • paraneooplatic syndrome (small cell CA of lung)
  • proximal
  • EMG
  • tx CA if present
  • starts at extremities moves up (MG starts at eyes and goes down), LE against voltage gated Ca and MG is at Ach receptors; LE weakness improves with activity and MG weakness worsens with activity; LE nerve stimulation will cause incremental response while MG will have decremental response
90
Q

Mult Sclerosis

  • epi
  • HLA
  • sxs
  • pathogeneis
  • Dx
  • CSF
  • tx: acute
  • Tx: long term
  • internuclear opthalmoplegia
  • types: relapsing remitting, primary progressive, secondary progressive, progressive- relapsing
A
  • middle aged females
  • DR15 and DQ6
  • scanning speech (break up syllables w pause), intention tremor, nystagmus
  • anti- myelin antibodies
  • MRI shows mult areas of demyelination with plaque like lesions
  • elevated IgG
  • IV corticosteroids
  • immuno modulators; IFN, natalizumab (decreases immune cell transmission), glatiramer (glutamate, lysine, alanine, tyrosine -> 4 components of myelin basic protein), mitoxantrone (topo 2 inhibitor), fingolimod (sequesters lymphocytes)
  • demyelination of MLF which is normally responsible for coordination of lateral conjugate gaze -> cant look laterally
  • acute attacks, then get better, and a little worse than before but pretty steady; steady increase in disability w/o acute attacks and no getting better; initally will relapse and remit but then have perios of getting worse without remission; steady decline with acute attacks
91
Q

Metachromatic leukodystrophy

  • caused by
  • what happens
  • epi
  • management
A
  • def of arylsulfatase A
  • affects growth and development of myelin -> MS in children
  • MS in 5-10 yr old
  • DMARDS
92
Q

Migraine

  • epi
  • last
  • sometimes contain
  • must have 2
  • must see 1
  • acute management
  • prophylaxis
A
  • female, 15-45 yrs; strong genetic component
  • 4-72 hrs
  • aura
  • unilateral, pulsatile, aggravated by movement, mod to severe in intensity, debilitating
  • n/v, photophobia, phonophobia
  • tyrpatan (5HT drugs)
  • Beta blocker
93
Q

Tension headache

  • side
  • quality
  • painful
  • related to
  • management
  • recurring
A
  • bilateral
  • band like
  • mild-mod, not debilitating
  • stress
  • avoid stressor, NSAID
  • amitryptilene
94
Q

Cluster Headache

  • side
  • characteristics
  • location
  • other sxs
  • tx
A
  • unilateral
  • 1-8 small HA per day, for 4-6 weeks
  • temporal/periorbital
  • ipsi rhinorrhea, miosis, eyelid edema
  • 100% O2 for 15 min, subcu triptans, prednisone
95
Q

Thunderclap headache

  • what is it
  • MCC
  • other sxs
  • complication, tx
A
  • severe headache, max intensity
  • rupture of Berry aneursym or AVM
  • fever, confusion and nuchal rigidity
  • arterial vasospasm 4-12 days after rupture -> cerebral ischemia -> focal neuro deficits and altered LOC; Ca channel blockers
96
Q

Infarction Terminology

  • stroke
  • TIA
  • lacunar infarct: what vessels, caused by
  • watershed infarct: location, caused by
  • embolic sources
  • global cerebral ischemia
  • when do you lose consiousness, neuronal activity stop, after 4-5 min
A
  • irreversible neuro deficit or reversible that does not resolve in less than 24 hours
  • transient ischemic attack -> reversible neuro deficit that resolves in less than 24 hours (usually 2-4 hours)
  • lenticulate striate vessels; chronic HTN or DM
  • occurs at border of 2 blood supplies; caused by prolonged hypotension
  • emboli from carotid, emboli from endocarditis
  • pt had MI and heart can’t pump blood so entire brain is losing blood supply
  • hypoxic for 5-10 sec, more than 1 min, permanent brain damage
97
Q

What happens w/ infarction

A
  • decrease in ATP -> noxic deploarization -> loss of membrane permeability -> glutamate released -> opening of NMDA and AMPA receptors -> Ca influx -> activation of catabolic enzymes and NO production -> cellular injury
98
Q

Lacunar infarct

  • what is it
  • caused by
  • diff from cerebral
  • pure motor
  • pure sensory
  • ataxia
  • dysarthria
A
  • ischemic infarct to small penetrating arterioles
  • chronic HTN and DM
  • will have both motor and sensory usually accompanied with broca or wernicke aphasia
  • posterior limb of internal capsule
  • VPM or VPL
  • base of pons
  • base of pons or genu of internal capsule
99
Q

Infarction presentation

  • MCA: what will be affected, if dominant side, if non dominant side
  • ACA
A
  • contralateral UE and facial motor and sensory loss; sup -> broca aphasia, inferior -> wernicke aphasia; contralateral hemi-neglect and apraxia
  • contralateral LE motor and sensory loss and ipsi blindness
100
Q

Histopath w. strokes

  • macro
  • micro
A
  • edema and blurring of grey and white matter junction

- red neurons, neutrophils and then macrophages, gliosis

101
Q

Dx and Management of stroke

  • imaging
  • LP
A
  • CT looking for bleed, if not then give TPA ; MRI after 24 hour to look for details; US of carotids
  • look for infection and r.o bleed
102
Q

Seizures

  • what is it
  • epilepsy
A
  • spontaneous and uncontrolled depolarization of brain

- recurring seizure of unknown cause

103
Q

Seizure Terminology

  • complex
  • simple
  • generalized
  • partial
  • tonic
  • clonic
  • petit mal (absence)
  • grand mal
A
  • LOC
  • no LOC
  • entire brain
  • focal
  • prolonged contraction
  • twitches
  • zoning out
  • complex, generalized, tonic-clonic seizure
104
Q

Seizure Work up

  • 1st
  • 2nd
  • 3rd
  • 4th
A
  • O2 (r/o ischemia causing seizure)
  • CT/MRI (r/o mass)
  • LP (r/o infection)
  • las (electrolyte abnormalities)
105
Q

Todds Paralysis

  • what is it
  • cause by
  • location
  • time frame
A
  • post-ictal paralysis
  • massive amount of ATP consumed during seizure -> decreased energy output of neurons and motor centers of brain
  • usually isolated to one side of body
  • 15-36 hrs
106
Q

Generalized Seizures

  • Tonic - Clonic: common, what happens, tx 1st line vs 2nd
  • Febrile: caused by, time frame, neuro sxs, EEG, age, tx
  • Myoclonic: sxs, tx
  • atonic: what happens, sxs, part of brain
  • benign rolandic: time frame, sxs,
  • lennox gastaut: age, what happens, sequelae
  • absence: epi, what happens, post ictal, time frame, EEG, tx
  • status epi: what is it, tx
A
  • most common; body stiffens/jerks; 1- valproate, 2- phenytoin or carbamazepine or lamotrigene and topiramate
  • caused by fever, less than 20 min, no neuro sxs before or after, EEG normal, 6m-6 yr, tylenol
  • pt experience full body muscular contractions; valproic acid
  • complete loss of muscle tone, pt falls to ground, frontal lobe
  • night time, one sided paresthesia and lose ability to speak, no recollection
  • childhood (2-6 yrs), expereince diff types of seizures on frequent basis; developmental delays and behaviorial problems
  • children, staring spell, none, 10s, 3hz spike and slow wave, ethosuximide
  • seizure lasting longer than 20 min, lorazepam or diazepam
107
Q

Focal Seizure

  • MCC
  • EEG
  • marching - jacksonian
  • temporal lobe: sxs, associated w/, tx
  • jacksonian: location, sxs
A
  • mass effect, stroke, infection
  • 3-spike pattern every second
  • seizure starts in motor cortex and marches through all muscles
  • psychomotor, associated w/ pre-seizure hallucinations, carbamazepine
  • primary cortex, move from side to side
108
Q

Anti-convulsive

  • Valproic Acid
  • Phenytoin
  • carbamazepine
  • Gabapentin
  • Tiagabine
  • Topiramate
  • Vigabatrin
  • lorazepam
  • myoclonic
  • partial
  • absence
  • tonic clonic
A
  • block voltage gated Na channels and increase GABA
  • block voltage gated Na channel; gingival hyperplasia, ataxia, nystagmus, hirsutism
  • NA channel blocker
  • increase GABA
  • inhibits GABA re-uptake
  • Blocks Na channels and increase GABA
  • increase GABA
  • benzo -> increases effect of GABA
  • valproate
  • carbamazepine
  • ethosuximide
  • phenytoin/carbamazepine/ valproate
109
Q

Prion Dx

  • Cruetzfield Jakob
  • PrP: what is it, what happens to it
A
  • accumulation of anormal prion; rapidly progressive dementia and myoclonic jerks
  • normally found in humans and has alpha helical structure but if it is converted into beta pleated sheet then proteins are resistant to proteases and accumulate in grey matter; causees spongiform changes and formation of vacuoles forming cysts that grow larger and larger