Neurological Disorders - ALS Flashcards

1
Q

What neurons does ALS affect?

A

Motor neurons

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2
Q

What do people with als often die from?

A

Respiratory failure

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3
Q

What are two other names for ALS?

A

Lougherigs and charcots

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4
Q

What three forms of ALS are there?

A

Sporadic
Familial
Other factors

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5
Q

How prevalent is the sporadic form of ALS and what are the two causes of it?

A

90-95%.
The SOD1 gene
Superoxide dimutase gene - mutation allows superoxide free radicals to accumulate and damage cells

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6
Q

What genes are involved in the familial etiology of ALS?

A

Sod1 gene and others

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7
Q

What other factors may contribute as an etiology to ALS?

A

Autoimmune

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8
Q

What is the patho of ALS? What is proposed as another patho for ALS?

A

Motor neurons are degenerated in: anterior horn cells in spinal cord, motor nuclei in brain stem and upper motor neurons in cerebral cortex

Free radical and or glutamate toxicity which results in damage to motor neurons

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9
Q

Where do upper motor neurons run from?

A

Brain to spinal cord

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10
Q

What are manifestations of ALS?

A

Muscle atrophy (because the muscle is receiving inadequate stimulation therefore person does not use)
Weakness
Fascicultations (spontaneous twitch)
Dysarthria (impaired speech)

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11
Q

What are the acute complications of ALS?

A

Dysphasia and aspiration

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12
Q

What remains intact in ALS?

A

Cognition and sensory function

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13
Q

How is ALS diagnosed?

A

Clinical presentation

Electromyography

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14
Q

What is the treatment for ALS?

A

Supporting management

Riluloze (neuro protective drug that addresses glutamate toxicity)

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15
Q

What three forms of ALS are there?

A

Sporadic
Familial
Other factors

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16
Q

How prevalent is the sporadic form of ALS and what are the two causes of it?

A

90-95%.

Superoxide dimutase gene (SOD1) - mutation allows superoxide free radicals to accumulate and damage cells

17
Q

What genes are involved in the familial etiology of ALS?

A

Sod1 gene and others

18
Q

What other factors may contribute as an etiology to ALS?

A

Autoimmune

19
Q

What is the patho of ALS? What is proposed as another patho for ALS?

A

Motor neurons are degenerated in: anterior horn cells in spinal cord, motor nuclei in brain stem and upper motor neurons in cerebral cortex

Free radical and or glutamate toxicity which results in damage to motor neurons

20
Q

Where do upper motor neurons run from?

A

Brain to spinal cord

21
Q

What are manifestations of ALS?

A

Muscle atrophy (because the muscle is receiving inadequate stimulation therefore person does not use)
Weakness
Fascicultations (spontaneous twitch)
Dysarthria (impaired speech)

22
Q

What are the acute complications of ALS?

A

Dysphasia and aspiration

23
Q

What remains intact in ALS?

A

Cognition and sensory function

24
Q

How is ALS diagnosed?

A

Clinical presentation

Electromyography

25
Q

What is the treatment for ALS?

A

Supporting management

Riluloze (neuro protective drug that addresses glutamate toxicity)