Case Info - BotMed Application

CaseName

Presentation Case 3. Gilbert syndrome

CaseDescription

he midst o f nal exams presents to a local clinic with “yellow eyes.” His
physical examination is unremarkable except or scleral icterus, and a
CBC and blood smear show no abnormalities. A comprehensive metabolic profile reveals a normal AST and ALT but elevated unconjugated bilirubin.

PhysicalExams

Labs

ImagingStudies

Comment

Gilbert syndrome is an autosomal recessive disorder o bilirubin glucuronidation due to ↓ activity of the enzyme glucuronyl trans erase.
Patients present with unconjugated hyperbilirubinemia but have a normal
CBC, blood smear, and LFTs. The condition is benign, and no treatment
is indicated.