apfcbAPFCB eNewscoAPFCB News Volume 3, Issue 1MultidisciplinaryEnglishJan-Jun, 2024NNY20240517ArticlesCASE-2: Gilbert syndrome diagnosticsEnglishY102105Dr. SumitaSharma1EnglishNDr. KapilSharma2EnglishYDr. Onjal K.Taywade1EnglishYDr ManishKumarand1EnglishY Dr. AnuragSankhyan1EnglishY10.62772/APFCB-News.2024.1.5Case HistoryAn 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.Englishhttps://apfcb.org/APFCB_News/abstract?id=5References16191. Torres L de S, Okumura JV, Silva DGH da, Bonini-Domingos CR. Hemoglobin D-Punjab: Origin, distribution and laboratory diagnosis. Rev Bras HematolHemoter. 2015;37(2):120and;ndash;6.2. Basmanj MT, Karimipoor M, Amirian A, Jafarinejad M, Katouzian L, Valaei A, et al. Co-inheritance of hemoglobin D and and;beta;-thalassemia traits in three Iranian families: Clinical relevance. Arch Iran Med. 2011;14(1):61and;ndash;3.3. Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis. 2010;5(1):1and;ndash;15.4. Vand;iacute;tek L, Tiribelli C. Gilbertand;acute;s syndrome revisited. J Hepatol. 2023;79(4):1049and;ndash;55.5. Petrenko AA, Pivnik A V, Kim PP, Demidova EY, Surin VL, Abdullaev AO, et al. Coinheritanceof HbD-Punjab/and;beta;+-thalassemia (IVSI+5 G-C) in a patient with Gilbertand;rsquo;s syndrome. Ter Arkh. 2018;90(7):105and;ndash;9.