Only diseases Flashcards

1
Q
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the most common hyperkinetic basal ganglia dysfunction?

what is the most common hypokinetic basal ganglia dysfunction?

A

Huntington’s Disease

Parkinson’s Disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is chorea?

what is athetosis?

what is dystonia?

what is ballismus?

A

rapid jerky involuntary movement

continued involuntary movement

locking muscles in a position

involuntary flinging of limbs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the cause of developing Huntington’s Disease?

why do we see the symptoms in this disease?

how do we categorize the symptoms seen in Huntington’s Disease?

A

loss of the ENK neurons of the striatum/neostriatum

Because the loss of ENK neurons allows the Globus Pallidus lateral to keep throwing GABA to the subthalamic nucleus…the globus pallidus medial does not get stimulated, the thalamus keeps active the cortex

Hyperkinetic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

When does Sydenham’s Chorea happen?

what ages are susceptible to this disease?

what are the symptom’s seen?

A

after following a viral infection, in particular Rheumatic Fever

ages 5-15

milkmaids grasp (rhythmic squeezing when the patient attempts to grab something), choreic hand, darting tongue and PRONATOR SIGN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

At what age does Parkinson’s Disease start?

What causes the symptoms to be seen in Parkinson’s Disease?

What can be seen in microscopy to identify Parkinson’s?

how do we categorize parkinson’s disease symptoms?

what are parkinson’s disease symptoms?

A

40-70

loss of neuromelanin due to loss of substantia negra

Lewy bodies

hypokinetic

resting tremor, bradykinesia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is Wilson’s Disease?

What are the symptoms of Wilson’s Disease?

In what part of the brian will the accumulation occur in wilson’s disease?

A

Copper accumulation in Liver, eyes, brain, kidneys due to a enzyme deficiency

fatigue, hepatitis, cirrhosis, behavioral changes, hypo or hyperkinetic movements, infertility, arrhytmias, Kayser-Fleischer rings

Copper accumulates in the lentiform nuclei

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what are the 3 types of cerebral palsy?

what gets damaged in each?

A
  1. spastic = corticospinal (motor cortex)
  2. ataxic = cerebellum
  3. athetoid or dyskinetic = basal ganglia damage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What do you see in a Anterior genu Lesion?

A

Akinetic mutism (patient doesnt move or talk)

tactile agnosia (cant sense things with touch)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What do you see with a Posterior Genu Lesion?

A

Alexia without agraphia: you can write but cant read)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is Somatoparaphrenia?

A

patient shows‘delusional’ misidentification, or confabulation, with regards to the affected limb

(“thats not my arm, but shes wearing my ring”)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is Asomatognosia?

what may cause it?

A
  • not perceiving one side of the body (or ignoring a part of the body)
  • neglect or paralysis of limb
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

say yes** or **no in each part of the table

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q
  1. what is visual agnosia?
  2. what is color agnosia?
  3. what is tactile agnosia?
  4. what is movement agnosia?
  5. what is anosognosia?
  6. what is autotopagnosia agnosia?
  7. what is statognosis?
  8. what is astereognosis?
  9. what is auditory agnosia?
  10. what is prosopagnosia?
A
  1. cant recognize an object visually
  2. cant name or distinguish colors
  3. cant recognize an object by touching it with either hand
  4. can’t determine objects that are static or moving
  5. can’t recognize that you have a disease
  6. can’t recognize a part of your own body
  7. can’t recognize spatial positioning of body parts
  8. tactile agnosia but in both arms
  9. cant recognize speech, animal sounds, mechanical sounds
  10. can’t recognize faces
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is constructional apraxia?

A

cannot reproduce an image

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what is this an example of?

A

neglect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

what is this an example of?

A

contructional apraxia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

what is this an example of?

A

contructional apraxia with neglect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what is neglect?

A

not recognizing an area of space

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

what is Papilledema?

A

non-inflammatory congestion of the optic disc

(papilla) due to increased intracranial pressure.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what is Retinitis Pigmentosa?

A

hereditary condition causing progressive deterioration of rods, resulting in loss of peripheral vision.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

what is Diabetic retinopathy?

A

Blood vessels swell, proliferate and distort. Will cause blindness if untreated.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

what is Proliferative retinopathy?

A

advanced form of diabetic retinopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

what do you get if the optic nerve is damaged?

what may cause optic nerve damage?

A

unilateral blindness

trauma and optic neuritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

what happens if you damage the lateral part of the Optic chiasm?

what may cause bilateral damage to the lateral optic chiasm?

what is the most common cause for damage to the lateral part of the optic chiasm?

A

binasal hemianopia

internal carotid aneurysm

calcified internal carotid arteries

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Damage to CN VI will result in?

there will be what type of diplopia? and only when looking in which direction?

A

Lack of abduction, medial deviation at rest (strabismus)

Horizontal diplopia only, when looking in direction of lesion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

what is 1 and a half syndrome?

A

Damage to abducens nucleus may only affect the lateral rectus itself; it may also affect the connections of abducens nucleus to the contralateral, CN III (lateral/horizontal conjugate gaze, reviewed in a few slides).

can result from damage to pons: leading

  • Ispilateral CN VI (lateral rectus).
  • MLF connection to ispilateral CN III (medial rectus).
  • MLF connection to contralateral CN III (medial rectus).
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

rostral MLF damage can cause what?

what happens if you damage the Frontal Eye Fields?

A

paralysis of vertical (upward) gaze (Parinauds)

there is no conjugate gaze to the lesioned side and inability of the eyes to look voluntarily to the opposite side.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

Damage to frontal eye fields, or PPRF, can be considered as?

A

supranuclear opthalmoplegia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

what is MLF Syndrome?

A

demyelination of the medial longitudinal fasciculus interrupts connections between CN III, IV, VI, and VIII.

basically Disconnection of CN III and VI interferes

with the lateral conjugate gaze.

32
Q

how will someone with CN 6 walk?

A
  1. dejected appearance: Patient will tilt head forward to compensate for difficulties in depressing the eye.
  2. Patient will tilt head to the side to compensate

for rotational problems (torsional diplopia). Head tilt is towards a nucleus, and away from a nerve, lesion.

33
Q

what is Aniscoria?

what is scotoma?

A

asymmetric pupils

blind spots in visual field

34
Q

what is a Argyl Robertson Pupil?

what may cause it?

A

an absence of direct and consensual light reflexes. Miotic reaction to accommodation/convergence is still intact

(doesnt react to light but do constrict in conversion)

syphilis, diabetes, and lupus.

35
Q

what is Foster Kennedy Syndrome?

what symptoms are seen?

A

Meningioma of the olfactory groove that compresses the olfactory tract and optic nerve

  1. ipsilateral anosmia
  2. optic atrophy
  3. contralateral papilledema.
36
Q

what is synesthesia?

A

condition wherein a stimuli for one sense is

perceived as another sense

(smell words)

37
Q

what is Anosmia?

what is hypo or hyper-osmia?

what is dysosmia?

what is parosmia?

what is phantosmia?

A
  • Loss of sensation of smell.
  • Diminished/enhanced sensation.
  • Distorted sensation.
  • Things smell worse than they should (occurs sometimes during upper respiratory infections).
  • Smelling something when there are no odors present (could be psychiatric i.e. schizophrenia,but also occurs with seizures and migraines).
38
Q

what is Olfactory Reference Syndrome (ORS):?

A

A persistent, false belief that one is emitting body

odors that are foul, and offensive to others.

The behavior of others is easily and often

misperceived (i.e. someone sniffs, or opens a

window, and the ORS person assumes it’s

because of them).

39
Q

what is Ageusia?

what is Hypogeusia?

what is Hypergeusia?

what is Dysgeusia?

what is Parageusia?

A
  • Loss of sense of taste
  • Diminished sensation
  • Enhanced sensation
  • Distorted sensation
  • Persistent abnormal taste
40
Q

what is pathological nystagmus?

A

If the eyes are showing movements when they aren’t

tracking anything, this is bad and indicates brainstem

or cerebellar damage.

41
Q

what is Conduction Deafness:?

what can cause it?

A

Interruption of the passage of sound waves through the outer and middle ear.

  1. Accumulation of cerumen (wax buildup).
  2. Otosclerosis: fixation of the stapes.
  3. Otitis media
42
Q

what is Sensorineural Deafness?

what leads to this?

A

Disease of the cochlea, cochlear nerve, or central auditory connections.

  1. Presbycusis
  2. Acoustic Neuroma
  3. Meniere’s Disease
  4. Hyperacusis
43
Q

What is the most common form of hearing loss?

A

Presbycusis

44
Q

what is Meniere’s Disease?

what symptoms will you see?

what can it result in?

A

Increased endolymph fluid pressure which enlarges the cochlear duct.

Results in episodes of fluctuating hearing loss

(distortions of the basilar membrane), tinnitus,

and recurrent vertigo lasting 30 mins - 24 hrs

can result in total loss

of hearing over a period of years

45
Q

what is Hyperacusis?

the condition is most commonly caused by what?

A

Paralysis of the stapedius muscle, or damage to CN VII, results in hyperacusis, where loud noises are not dampened.

by exposure to loud noises/environments

46
Q

how do you know a patient has conductive hearing loss with Weber’s test?

how do you know a patient has sensorineural hearing loss with Weber’s test?

A

place tuning fork in forehead and patient will hear it louder in one side of the ear

patient will hear the sound louder in the unaffected ear.

47
Q

how do you know a patient has conductive hearing loss using Rinne’s test?

how do you know a patient has sensorineural hearing loss using Rinne’s test?

A

Conductive: BC better than AC.

Sensorineural: Both AC and BC are depreciated.

48
Q

what is Tinnitus?

A

‘ringing in the ears’ is the sensation of hearing ringing, buzzing, hissing, chirping, whistling, or other sounds. The noise can be intermittent or continuous, and varies in loudness

49
Q

what is misphonia?

A

“Hatred of Sound”: A strong negative emotional

response triggered by specific sounds. Often

accompanied by a flight response.

50
Q

Migraines typically have four stages:

A
  1. Prodrome: symptoms occuring 1-2 days before the attack
  2. Aura: Visual most = Scintillating scotoma (curved blind spot)
  3. Attack: 4-72 hours
  4. Postdrome: 1-2 days, feeling drained/exhausted.
51
Q

Common Migrane headaches are present at least how many days a month?

for how many months?

how many days do migranes have to occur to be considered episodic migranes ?

A

more than 15

3 months

less than 15

52
Q

Coital migraines:

occur more on which sex?

the onset occurs when?

is very similar to what other disease?

what are its 3 presentations?

A

men

at orgasm

subarachnoid hemmorrhage

  1. Early = pain increases proportional to excitation
  2. Orgasmi = at orgasm
  3. late = after orgasm
53
Q

Temporal arteritis occurs do to what?

what symptoms does it present with?

happens on which sex most commonly?

what is another name for this? when is it called this?

can cause what?

A

inflammation of large blood vessels

Tender scalp and pain with chewing

women

Giant cell arteritis

when it affects neck, shoulder, upper arms

stroke

54
Q

what are Cluster headaches?

some symptoms are?

what helps reduce the pain?

A

group of headaches with pain over 1 eye, everyday at the same time in the same location

droopy eyelid, red eye

walking around

55
Q

what is Hemicranium continua?

how do you treat?

A

similar to cluster headache but with higher frequency of attacks with shorter duration

Indomethacin

56
Q

what are Tension headaches?

what do you treat?

how do you treat chronic tension headaches?

A

headache caused by stress, fatigue, dehydration, bad posture, hunger

analgesics

anti-depressants

57
Q

what is New Onset Persistent Daily headache?

lasts how long?

A

similar to chronic migraine or tension headaches but it doesnt go away

months

58
Q

what is Complex regional pain syndrome?

what is another name for this?

A

Burning pain and hypersensitivity to temperature in affected areas, resulting from trauma or nerve damage.

RSD (Reflex Sympathetic Dystrophy

59
Q

an example of Post stroke chronic pain?

another name for this is?

what part of the body does it affect?

how does it present?

A

Thalamic Pain Syndrome

(Dejerine-Roussy Syndrome)

Pain affecting contralateral side of body

Occurs some time (weeks-month) after the initial infarct/damage to thalamus. numbness first, then pain

60
Q

Where do Epileptic Seizures start?

what should we remember about non-epileptic seizures?

Non-epileptic seizures can be divided into what?

A

the brain

they dont happen by changes in brain electrical activity

Can be divided into Organic NES, and Psychogenic NES.

61
Q

what are the types of epileptic seizures?

A
  1. Generalized seizures
  2. Generalized tonic clonic
  3. Myoclonic
  4. Absence
  5. Atonic
62
Q

how do we define a generalized seizures?

A

Affect both hemispheres from the beginning of the seizure.

Loss of consciousness occurs for varying periods of time.

63
Q

how do we define a Generalized tonic clonic?

A

‘Grand Mal’. Tonic phase includes stiffening of the limbs, clonic phase is jerking of the limbs and face.

64
Q

how do we define a myoclonic seizure?

hwo do we define an absence seizure?

A

Rapid, brief contraction of body muscles. Usually involves arms or feet/legs (both sides of body)

Periods of lack of awareness, usually lasting less than a minute.

65
Q

what is another name for absence seizure?

how do we define atonic seizure?

A

‘Petit Mal

Abrupt loss of muscle tone.

66
Q

what is Myoclonus?

is it normal or abnormal?

A

Brief, involuntary twitching of a muscle or a group of muscles.

normal

67
Q

what are Types of Epileptic Seizures (Partial)?

how do we differenciate each?

what is a partial seizure?

A

Simple partial involves no loss of consciousness. Complex partial consciousness is lost or impaired.

partial seizure: area of seizure is limited to one region of the body.

68
Q

what is Pre-eclampsia?

What is Eclampsia?

A
  • High blood pressure and elevated levels of protein in urine in pregnant women.
  • Tonic-clonic seizures (the eclamptic convulsion).
69
Q

what is the Leading cause of maternal and peri-natal death?

A

Eclampsia

70
Q

what is the Treatment of Seizures?

A
  1. Anticonvulsant meds: Dilantin (phenytoin), Tegretol (carbamazepine); many many more.
  2. Surgical removal of focal area (if a focal area can be identified).
  3. Diet restrictions (i.e. young children with phenylketonuria). ‘The Ketogenic Diet’
  4. Vagus nerve stimulation (VNS): Stimulating

electrode ‘wrapped’ around the left vagus

nerve (less cardiac effects than the right).

71
Q

what is another name for Psychogenic non-epileptic seizures?

how do you treat this type?

A

dissociative seizures

do not originate from physical causes, thus are treated with therapy and often adjunct meds

72
Q

5-HT depletion will cause?

A

insomnia

73
Q

what is cauda equina syndrome?

symptoms present where?

what symptoms do we see?

A

compression of cauda equina

below the compression

paralysis, sensory loss, parasthesia, bladder control loss

74
Q

what is Sciatica?

what nerves does it involve?

A

collection of symptoms. Caused by compression of sciatic nerve

L4, L5, S1, S2, S3