MS And MND Flashcards

1
Q

What is MS

A

An auto immune disease affecting the CNS as myelin is damaged

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2
Q

What is an auto immune disease

A

When the immune system is directed towards the body’s own cells

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3
Q

What is the average onset age for MS

A

20-30 years

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4
Q

Name some genetic factors relating to MS

A

2x more women
More Caucasian
If both parents have the disease children have a 20% chance of having it

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5
Q

Percentage facts about MS

A

50% after 20 years of being diagnosed will need a walking stick
50% have some cognitive involvement
Life expectancy reduced by 10-15 years

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6
Q

Name some environmental factors relating to MS

A

5x more likely in colder climates
Infections can bring on onset
Vitamin D deficiencies

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7
Q

Name some symptoms of MS

A
fatigue 
Visual loss 
Depression 
Tremor
Speech disturbance 
Pain
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8
Q

What is the difference between primary, secondary and systemic fatigue

A

Primary- increased effort to perform tasks
Secondary- depression, sleep disturbances
Systemic- chronic lack of energy

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9
Q

What is MS differentially diagnosed from and what tests are done?

A
Lyme disease 
B-12 deficiency 
Tests-
Lumbar puncture 
Neurological exam
Brain imaging
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10
Q

Describe the different stages/ forms of MS

A

Primary progressive -15%
-Symptoms gradually get worse
Relapsing Remitting
-episodes occur followed by a period of some possible recovery (weeks/ months) this is the most common
Secondary Progressive
- begins as relapsing remitting but over time symptoms remain present and get worse
Progressive relapsing
- symptoms steadily get worse but episodes may or may not be followed by a period of recovery. This is the least common

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11
Q

What is the difference between benign and malignant MS

A
-Malignant (acute)- progresses rapidly leading to disability in short period of time
Rare
-Benign 
15 years or more with no disability 
Little progression after first attack
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12
Q

Describe MS treatment

A
  • interferon beta 1a and 1b ( protein replicates human interferon)
  • Glatiramer Acetate ( resembles protein in myelin)
    Drugs combined reduce relapse by 33%
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13
Q

What is MND

A

When messages from neurons become less functional

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14
Q

What is ALS

A

Amyotrophic lateral schlerois
Upper and lower MN signs
80% develop bulbar involvement
Speech affected before swallowing

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15
Q

What is progressive bulbar palsy

A

Makes up for 20% of MND cases
Speech and swallowing early features (6-12 months complete inability to produce speech)
Life expectancy 2-4 years

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16
Q

What is progressive muscular atrophy

A

Lower MN predominant
Upper MN develop at some point
Life Expectancy- 5 years

17
Q

What is primary lateral schlerosis

A
1-2% of cases 
Spastic tetraparesis 
Loss of speech within 3 years
Urinary urgency 
Long survival rate
18
Q

What is flail arm MND

A
  • bilateral weakness in upper limbs
  • may not spread for a number of years
  • males more affected
19
Q

Lower limb onset

A

Also known as creeping paralysis

Gradual ascending distal weakness

20
Q

What drugs can be used for MND

A

Riluzole

It is a glutamate inhibitor which can prolong life by 3-6 months