Exploring a Case of Unconjugated Hyperbilirubinaemia Resulting from the Rare Coexistence of Inherited Disorders- A Case Report

Author:

Sharma Sumita,Sharma KapilORCID,Taywade Onjal K.,Kumar Manish,Sankhyan Anurag

Publisher

Springer Science and Business Media LLC

Reference9 articles.

1. Torres Lde S, Okumura JV, Silva DG, Bonini-Domingos CR. Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis. Rev Bras Hematol Hemoter. 2015;37(2):120–6. https://doi.org/10.1016/j.bjhh.2015.02.007.

2. Basmanj MT, Karimipoor M, Amirian A, Jafarinejad M, Katouzian L, Valaei A, et al. Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance. Arch Iran Med. 2011;14(1):61–3.

3. Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis. 2010;5(1):1–15.

4. Vítek L, Tiribelli C. Gilbert’s syndrome revisited. J Hepatol. 2023;79(4):1049–55. https://doi.org/10.1016/j.jhep.2023.06.004.

5. Petrenko AA, Pivnik AV, Kim PP, Demidova EY, Surin VL, Abdullaev AO, et al. Coinheritance of HbD-Punjab/β+-thalassemia (IVSI+5 G-C) in patient with Gilbert’s syndrome. Ter Arkh. 2018;90(7):105–9.

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