Understanding Amyotrophic Lateral Sclerosis (ALS)

Understanding Amyotrophic Lateral Sclerosis (ALS)

Assessment

Interactive Video

Biology, Science

9th - 12th Grade

Hard

Created by

Ethan Morris

FREE Resource

This video provides a concise overview of amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. It explains the symptoms, progression, and survival statistics of the disease. ALS is a neurodegenerative disorder affecting upper and lower motor neurons, leading to muscle spasticity and weakness. The video discusses the unknown causes of ALS, the role of genetic mutations, and the accumulation of dysfunctional proteins in neurons. It highlights the complexity of ALS and the multiple mechanisms that may contribute to neurodegeneration.

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9 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is another name for ALS in the United States?

Lou Gehrig’s disease

Multiple sclerosis

Huntington's disease

Parkinson's disease

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is a common symptom as ALS progresses?

Increased appetite

Enhanced cognitive function

Improved muscle strength

Difficulty in breathing

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the average survival time after an ALS diagnosis?

6-8 years

10-12 years

1-2 years

3-5 years

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which neurons are primarily affected in ALS?

Upper and lower motor neurons

Interneurons

Autonomic neurons

Sensory neurons

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of lower motor neurons?

Connect different parts of the brain

Extend from the spinal cord to skeletal muscles

Transmit sensory information to the brain

Regulate autonomic functions

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a characteristic feature of ALS similar to Alzheimer's disease?

Rapid cell regeneration

Increased neuron connectivity

Accumulation of dysfunctional proteins

Enhanced memory retention

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the current understanding of the genetic mutations linked to ALS?

Their effects are not completely clear

They have no effect on ALS

They are completely understood

They prevent ALS

8.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is hypothesized about the protein aggregates found in ALS?

They are beneficial for neurons

They enhance neuronal function

They have no impact on neurons

They could impair neuronal function

9.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How many mechanisms are likely involved in ALS neurodegeneration?

More than one

Only one

None

Exactly two