Gilbert Syndrome | Causes (Genetics), Pathogenesis, Signs & Symptoms, Diagnosis, Treatment

Gilbert Syndrome | Causes (Genetics), Pathogenesis, Signs & Symptoms, Diagnosis, Treatment

Assessment

Interactive Video

Health Sciences, Biology

University - Vocational training

Hard

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The video tutorial explains Gilbert syndrome, a benign genetic condition causing recurrent jaundice due to unconjugated hyperbilirubinemia. It covers the pathophysiology involving the UGT gene and UDP glucuronyl transferase enzyme, the epidemiology affecting 3-7% of the population, and the clinical features like jaundice triggered by stress or fasting. Diagnosis involves blood tests showing high unconjugated bilirubin levels, and no treatment is required as the condition is benign.

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3 questions

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1.

OPEN ENDED QUESTION

3 mins • 1 pt

What is the role of the enzyme UDP glucuronyl transferase in Gilbert syndrome?

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2.

OPEN ENDED QUESTION

3 mins • 1 pt

What is the epidemiology of Gilbert syndrome in the general population?

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3.

OPEN ENDED QUESTION

3 mins • 1 pt

What treatment options are available for individuals diagnosed with Gilbert syndrome?

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