neuromuscular disease Flashcards

1
Q

what are the main types of anterior horn cell disease ?

A

primary disease of motor neurons

spinal cord pathology

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

what disease fall under primary disease of motor neurons?

A

MND
ALS
poliomyelitis

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

what diseases fall under spinal cord pathology ?

A

spinal cord infarction

syringomyelia

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

UMN and LMN ?

A

ALS

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

pure UMN ?

A

primary lateral sclerosis

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

pure LMN ?

A

progressive muscular atrophy

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

how to differentiate between bulbar and pseudo bulbar ?

A

tongue depressor test

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

what medication can be given for MND ?

A

riluzole

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the single causes of mixed UMN and LMN signs?

A
freds- fredrich ataxia 
tabby- taboporesis 
cat - cervical spondylosis 
seeks - subacute combined degeneration of the cord 
mice - motor neuron disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what could be the cause of subacute combined degeneration of the cord ?

A

B12 deficiency

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

what could be the cause of taboporesis ?

A

syphillus

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

what is cauda equina syndrome ?

A

severe type of spinal stenosis and the symptoms include sciatica on both sides. weakness or numbness in both legs along with numbness around or under your genitals, or around your anus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what are myotomes ?

A

muscles supplied by spinal cord

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is the most common example of hereditary sensory and motor neuropathy neuropathy ?

A

charcot marie tooth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the types of charcot marie tooth ?

A

type 1 which is demyelinating

type 2 which is axonal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what type of disease is guilliane barre ?

A

an autoimmune demyelinating disease

17
Q

what is the chronic form of GBS ?

A

CIDP
chronic inflammatory demyelinating polyradiculopathy
>8 weeks frrom onset

18
Q

what is the nature of pain in small fibre neuropathy ?

A

painful and burning sensations nerve conduction is usually normal

19
Q

what is the most common nerve affected in DM ?

A

Cranial mononeuropathy III

20
Q

what is the disease course like in CIDP ?

A

relapsing remitting

21
Q

what is the genetic abnormality in CMT ?

A

PMP22 gene duplication

22
Q

what is the weakness like in CMT ?

A

progressive distal weakness

23
Q

what is Gullian barre syndrome often precipitated by ?

A

infection such as viral or campylobacter , post vaccination

aw ay 7aga respiratory or GIT

24
Q

what is the presentation in gullian barre ?

A

Progressive ascending symmetrical limb weakness (usually starting with the lower limbs)
Lower back pain due to radiculopathy
Paraesthesia, often preceding motor symptoms
lower motor neeuurron signs

25
Q

what can be done to treat GBS ?

A

IVIg

26
Q

what type of neuromuscular disease does lyme disease cause ?

A

non compressive radiculopathy

27
Q

what is the presentation of Charcot marie tooth disease ?

A

onset is usually at puberty , starts with affection of the feet then makes its way to thee hands
champagne bottle legs
pes cavus
claw hand

28
Q

what are the signs of LMNL ?

A

hypotonia
flaccid paralysis

29
Q

what is miller fisher syndrome ?

A

one of the forms of GBS and is associated with anti-GQ1B antibodies

30
Q

what is usually found in the CSF of patients with GBS ?

A

Albuminocytologic dissociation

31
Q

fasiculations are characteristic of which level of affection ?

A

AHC

32
Q

diurnal variation associated with which level of affection ?

A

NMJ