{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T01:52:55Z","timestamp":1762393975001,"version":"build-2065373602"},"reference-count":15,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,11,5]]},"DOI":"10.7759\/cureus.96168","type":"journal-article","created":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T01:49:19Z","timestamp":1762393759000},"source":"Crossref","is-referenced-by-count":0,"title":["Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India"],"prefix":"10.7759","author":[{"given":"Rizwan","family":"Athar","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rajesh","family":"Kashyap","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jalaj","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1182\/blood.V94.7.2259.419k42_2259_2262","article-title":"Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis","volume":"94","author":"del Giudice EM","year":"1999","unstructured":"del Giudice EM, Perrotta S, Nobili B, Specchia C, d\u2019Urzo G, Iolascon A. Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. Blood. 1999, 94:2259-62. 10.1182\/blood.V94.7.2259.419k42_2259_2262","journal-title":"Blood"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.4240\/wjgs.v17.i7.105033","article-title":"Association between hereditary spherocytosis and gallstone disease: pathophysiology, diagnosis, and management","volume":"17","author":"Cong S","year":"2025","unstructured":"Cong S, Wang YN, Wang JR, Duan RH. Association between hereditary spherocytosis and gallstone disease: pathophysiology, diagnosis, and management. World J Gastrointest Surg. 2025, 17:105033. 10.4240\/wjgs.v17.i7.105033","journal-title":"World J Gastrointest Surg"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1002\/jcla.24034","article-title":"The diagnostic protocol for hereditary spherocytosis-2021 update","volume":"35","author":"Wu Y","year":"2021","unstructured":"Wu Y, Liao L, Lin F. The diagnostic protocol for hereditary spherocytosis-2021 update. J Clin Lab Anal. 2021, 35:24034. 10.1002\/jcla.24034","journal-title":"J Clin Lab Anal"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1080\/10245332.2018.1455278","article-title":"Analysis of erythrocyte membrane proteins in patients with hereditary spherocytosis and other types of haemolytic anaemia","volume":"23","author":"Shibuya A","year":"2018","unstructured":"Shibuya A, Kawashima H, Tanaka M. Analysis of erythrocyte membrane proteins in patients with hereditary spherocytosis and other types of haemolytic anaemia. Hematology. 2018, 23:669-75. 10.1080\/10245332.2018.1455278","journal-title":"Hematology"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1016\/j.blre.2013.04.003","article-title":"Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders","volume":"27","author":"Da Costa L","year":"2013","unstructured":"Da Costa L, Galimand J, Fenneteau O, Mohandas N. Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders. Blood Rev. 2013, 27:167-78. 10.1016\/j.blre.2013.04.003","journal-title":"Blood Rev"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.12998\/wjcc.v8.i10.2001","article-title":"Gilbert's syndrome coexisting with hereditary spherocytosis might not be rare: six case reports","volume":"8","author":"Kang LL","year":"2020","unstructured":"Kang LL, Liu ZL, Zhang HD. Gilbert's syndrome coexisting with hereditary spherocytosis might not be rare: six case reports. World J Clin Cases. 2020, 8:2001-8. 10.12998\/wjcc.v8.i10.2001","journal-title":"World J Clin Cases"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.14218\/JCTH.2023.00563","article-title":"Genetics of gallstone disease and their clinical significance: a narrative review","volume":"12","author":"Costa CJ","year":"2024","unstructured":"Costa CJ, Nguyen MT, Vaziri H, Wu GY. Genetics of gallstone disease and their clinical significance: a narrative review. J Clin Transl Hepatol. 2024, 12:316-26. 10.14218\/JCTH.2023.00563","journal-title":"J Clin Transl Hepatol"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1038\/ncpgasthep0257","article-title":"Mechanisms of disease: the genetic epidemiology of gallbladder stones","volume":"2","author":"Lammert F","year":"2005","unstructured":"Lammert F, Sauerbruch T. Mechanisms of disease: the genetic epidemiology of gallbladder stones. Nat Clin Pract Gastroenterol Hepatol. 2005, 2:423-33. 10.1038\/ncpgasthep0257","journal-title":"Nat Clin Pract Gastroenterol Hepatol"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1055\/s-0031-1276645","article-title":"Dissecting the genetic heterogeneity of gallbladder stone formation","volume":"31","author":"Krawczyk M","year":"2011","unstructured":"Krawczyk M, Wang DQ, Portincasa P, Lammert F. Dissecting the genetic heterogeneity of gallbladder stone formation. Semin Liver Dis. 2011, 31:157-72. 10.1055\/s-0031-1276645","journal-title":"Semin Liver Dis"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.2011.08921.x","article-title":"Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update","volume":"156","author":"Bolton-Maggs PH","year":"2012","unstructured":"Bolton-Maggs PH, Langer JC, Iolascon A, Tittensor P, King MJ. Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update. Br J Haematol. 2012, 156:37-49. 10.1111\/j.1365-2141.2011.08921.x","journal-title":"Br J Haematol"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1515\/med-2022-0549","article-title":"Association of gallstone and polymorphisms of UGT1A1*27 and UGT1A1*28 in patients with hepatitis B virus-related liver failure","volume":"17","author":"Zhuo H","year":"2022","unstructured":"Zhuo H, Fan J, Zhang B, Shi Y, Zheng L, Chai Y, Yao L. Association of gallstone and polymorphisms of UGT1A1*27 and UGT1A1*28 in patients with hepatitis B virus-related liver failure. Open Med (Wars). 2022, 17:1455-65. 10.1515\/med-2022-0549","journal-title":"Open Med (Wars)"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1016\/B978-0-12-812532-8.00019-7","article-title":"Bile pigment metabolism and its disorders","author":"Roy-Chowdhury N","year":"2020","unstructured":"Roy-Chowdhury N, Wang X, Roy-Chowdhury J. Bile pigment metabolism and its disorders. Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics. Elsevier, Amsterdam, Netherlands; 2020. 507-53. 10.1016\/B978-0-12-812532-8.00019-7"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.14218\/JCTH.2024.00156","article-title":"The multifaceted role of bilirubin in liver disease: a literature review","volume":"12","author":"Ram\u00edrez-Mej\u00eda MM","year":"2024","unstructured":"Ram\u00edrez-Mej\u00eda MM, Castillo-Casta\u00f1eda SM, Pal SC, Qi X, M\u00e9ndez-S\u00e1nchez N. The multifaceted role of bilirubin in liver disease: a literature review. J Clin Transl Hepatol. 2024, 12:939-48. 10.14218\/JCTH.2024.00156","journal-title":"J Clin Transl Hepatol"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.24953\/turkjped.2018.03.005","article-title":"Hereditary spherocytosis: retrospective evaluation of 65 children","volume":"60","author":"G\u00fcng\u00f6r A","year":"2018","unstructured":"G\u00fcng\u00f6r A, Yaral\u0131 N, Fettah A, Ok-Bozkaya \u0130, \u00d6zbek N, Kara A. Hereditary spherocytosis: retrospective evaluation of 65 children. Turk J Pediatr. 2018, 60:264-9. 10.24953\/turkjped.2018.03.005","journal-title":"Turk J Pediatr"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1097\/MPH.0000000000002211","article-title":"Clinical features and outcome of children with hereditary spherocytosis","volume":"44","author":"Kili\u00e7 MA","year":"2022","unstructured":"Kili\u00e7 MA, \u00d6zdemir GN, Tahtakesen TN, et al.. Clinical features and outcome of children with hereditary spherocytosis. J Pediatr Hematol Oncol. 2022, 44:306-9. 10.1097\/MPH.0000000000002211","journal-title":"J Pediatr Hematol Oncol"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/375176-confounding-factors-in-the-diagnosis-of-hereditary-spherocytosis-and-gallstone-formation-in-related-hemolytic-disorders-from-a-tertiary-care-center-in-north-india","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T01:49:19Z","timestamp":1762393759000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/375176-confounding-factors-in-the-diagnosis-of-hereditary-spherocytosis-and-gallstone-formation-in-related-hemolytic-disorders-from-a-tertiary-care-center-in-north-india"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,11,5]]},"references-count":15,"URL":"https:\/\/doi.org\/10.7759\/cureus.96168","relation":{},"ISSN":["2168-8184"],"issn-type":[{"type":"print","value":"2168-8184"}],"subject":[],"published":{"date-parts":[[2025,11,5]]}}}