CASE-2: Gilbert syndrome diagnostics

Pages: 102-105

Dr. Sumita Sharma1, Dr. Kapil Sharma2, Dr. Onjal K. Taywade1, Dr Manish Kumarand1, Dr. Anurag Sankhyan1

1Department of Biochemistry, All India Institute of Medical Sciences, Bilaspur, Himachal Pradesh,India

2Department of General Medicine, All India Institute of Medical Sciences, Bilaspur, Himachal Pradesh, India

Corresponding Author: Dr. Sumita Sharma
Email: drsumita17@gmail.com

Abstract

Case History

An 18-year-old female presented to General Medicine OPD for evaluation of jaundice. The patient had a history of intermittent jaundice for the last one year. At the time of presentation,there was no history of fever, anorexia, weight loss, dark urine, clay-coloured stool, pruritus, pain abdomen, abdominal distension or pedal swelling. She did not have a history of any chronicdisease or blood transfusion and her family history was not significant for any chronic disease.On physical examination, mild pallor and mild icterus were noticed. There was neither any lymphadenopathy nor hepatosplenomegaly. Cardiovascular and central nervous system examination was normal.