Creutzfeldt-Jakob Disease (CJD): An Overview of Symptoms, Causes, & Diagnosis

Creutzfeldt-Jakob Disease (CJD): An Overview of Symptoms, Causes, & Diagnosis

Assessment

Interactive Video

Biology

10th - 12th Grade

Hard

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The video explains the role of proteins in neuron function and introduces Creutzfeldt-Jakob Disease (CJD), a rare prion disease. It describes the symptoms, including rapidly progressive dementia, myoclonus, and ataxia. The video details how prion proteins misfold, leading to cell death, and outlines the four types of CJD: sporadic, familial, iatrogenic, and variant. Diagnosis methods like EEG, MRI, and CSF analysis are discussed, along with the disease's progression and prognosis. The video concludes with a case study of a patient named Anthony, who succumbed to CJD.

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3 questions

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1.

OPEN ENDED QUESTION

3 mins • 1 pt

What diagnostic methods were used to confirm Anthony's condition?

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2.

OPEN ENDED QUESTION

3 mins • 1 pt

What is the significance of the 1433 protein in relation to Creutzfeldt-Jakob Disease?

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3.

OPEN ENDED QUESTION

3 mins • 1 pt

Discuss the prognosis for individuals diagnosed with Creutzfeldt-Jakob Disease.

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