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Gilbert Syndrome in a Young Ethiopian Man: First Case Report
Amir Sultan1, Kibrewossen Kiflu2
1Addis Ababa University, College of Health Sciences, Division of Gastroenterology & Hepatology, Addis Ababa, Ethiopia https://orcid.org/0000-0002-7000-9575.
Background:
Gilbert syndrome is a well-recognized condition causing unconjugated hyperbilirubinemia with otherwise normal transaminases and liver function tests.
Case:
A 21 year old male patient presented with recurrent episodes of jaundice over four years. The episodes were preceded by stressful conditions and intercurrent illnesses. All laboratory prameters were normal except an unconjugated hyperbilirubinemia. A diagnosis of Gilbert syndrome was made after careful clinical evaluation.
Conclusion:
Recognizing Gilbert syndrome has important clinical implicaitions by avoiding uncessary and expensive workup of patients with jaundice. Mangement entails avoiding stressful conditions and prolonged fasting.

