Physiology Flashcards

1
Q

A Focal/Partial seizure is proceeded by what phenomena? How does it begin physiologically?

A

Aura-sense of fear

Starts with small group of localized neuron which have the potential to spread and generalize.

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2
Q

How are generalized and focal seizures distinguished?

A

Focal-proceeded by aura, start localized and spread

Generalized-No aura, bilateral from onset

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3
Q

A childhood absence seizure is of what type? What regions of the brain does it involve. How is it unique?

A

Generalized
thalamocortical circuts
Diffuse hyperexcitability
No aura

Unique-inhibition is preserved, but the depolarization and hyperpolarization phases become stronger.

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4
Q

The metabolic demands during a partial seizure lead to a 3 fold increase in glucose and O2 which can be detected with imaging techniques. What’s important to remember when considering these effects?

A

That seizures don’t stop b/c of this

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5
Q

What is status epilepticus?

A

Repeated generalized seizures without a return to full consciousness or about 5-10 mins of continuous convulsive seizures.

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6
Q

How do you get brain damage from seizures?

A

Excitotoxicity from excessive glutamate release and increases in intracellular Ca2+, enzymes, free radicals, and apoptosis, as well as Na+ influx and edema.

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7
Q

Why is the limbic system particularly susceptible to seizure?

A

The hippocampus especially has a lot of feed forward signals….

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8
Q

What is Ohtahara Syndrome

A

It’s a infantile epileptic encephalopathy.
Most severe and and earliest developing in children
Tonic spasms are the main seizure observed

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9
Q

What are some examples of severe myoclonic epilepsy in infancy?

A

Dravet Syndrome

Lennox-Gaustaut syndrome

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10
Q

What is Dravet syndrome?

A

Severe form of myoclonic epilepsy characterized by onset in first year of life. Leads to developmental delay and persistant gait ataxia, and cognitive and behavioral imparement.
Mortality rate is 10%
Very few patients develop normally

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11
Q

What is Lennox-Gaustaut Syndrome

A

Severe form of myoclonic epilepsy characterized by mental retardation and psychotic symptoms. Usually the result of brain damage from seizure.
2-9 y/o

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12
Q

What is Landau-Kleffner syndrome?

A

Epileptic aphasia
VERY RARE
3-6 y/o
Child begins to loose language function, act deaf

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13
Q

How could ion channel, neurotransmitter development, and electrical synapses contribute to childhood seizures?

A

depolarizing channels and excitatory neurotransmitters develop first, and there are also more electrical synapses during childhood.

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