{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T15:55:05Z","timestamp":1762444505822,"version":"build-2065373602"},"reference-count":21,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2015,2,1]],"date-time":"2015-02-01T00:00:00Z","timestamp":1422748800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"name":"Provincial Natural Science Foundation of Guangxi","award":["2011GXNSFA018290"],"award-info":[{"award-number":["2011GXNSFA018290"]}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinica Chimica Acta"],"published-print":{"date-parts":[[2015,2]]},"DOI":"10.1016\/j.cca.2014.12.002","type":"journal-article","created":{"date-parts":[[2014,12,6]],"date-time":"2014-12-06T22:16:46Z","timestamp":1417904206000},"page":"6-9","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"special_numbering":"C","title":["Misdiagnosis of two cases of hereditary spherocytosis in a family and review of published reports"],"prefix":"10.1016","volume":"441","author":[{"given":"Zengfu","family":"Deng","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lin","family":"Liao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wang","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Faquan","family":"Lin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.cca.2014.12.002_bb0005","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1111\/j.1365-2141.2011.08921.x","article-title":"Guidelines for the diagnosis and management of hereditary spherocytosis\u20142011 update","volume":"156","author":"Bolton-Maggs","year":"2012","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.cca.2014.12.002_bb0010","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1016\/j.blre.2013.04.003","article-title":"Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders","volume":"27","author":"Da Costa","year":"2013","journal-title":"Blood Rev."},{"key":"10.1016\/j.cca.2014.12.002_bb0015","doi-asserted-by":"crossref","first-page":"759","DOI":"10.1007\/s00277-010-1138-3","article-title":"Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study","volume":"90","author":"Mullier","year":"2011","journal-title":"Ann. Hematol."},{"key":"10.1016\/j.cca.2014.12.002_bb0020","doi-asserted-by":"crossref","first-page":"421","DOI":"10.7754\/Clin.Lab.2012.120905","article-title":"A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemia","volume":"59","author":"Vercellati","year":"2013","journal-title":"Clin. Lab."},{"key":"10.1016\/j.cca.2014.12.002_bb0025","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/j.tracli.2010.05.006","article-title":"Hereditary spherocytosis","volume":"17","author":"Iolascon","year":"2010","journal-title":"Transfus. Clin. Biol."},{"key":"10.1016\/j.cca.2014.12.002_bb0030","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1186\/1756-0500-7-137","article-title":"Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literature","volume":"7","author":"Kobayashi","year":"2014","journal-title":"BMC Res. Notes"},{"key":"10.1016\/j.cca.2014.12.002_bb0035","first-page":"54","article-title":"Hereditary spherocytosis in a malay patient with chronic haemolysis","volume":"14","author":"Sheikh","year":"2007","journal-title":"Malays J. Med. Sci.: MJMS"},{"key":"10.1016\/j.cca.2014.12.002_bb0040","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1586\/ehm.12.3","article-title":"Hemolytic anemia in adults: main causes and diagnostic procedures","volume":"5","author":"Guillaud","year":"2012","journal-title":"Expert Rev. Hematol."},{"key":"10.1016\/j.cca.2014.12.002_bb0045","doi-asserted-by":"crossref","first-page":"560","DOI":"10.1016\/j.autrev.2013.11.010","article-title":"Diagnosis and classification of autoimmune hemolytic anemia","volume":"13","author":"Bass","year":"2014","journal-title":"Autoimmun. Rev."},{"key":"10.1016\/j.cca.2014.12.002_bb0050","doi-asserted-by":"crossref","first-page":"5","DOI":"10.4103\/0973-6247.126681","article-title":"Autoimmune hemolytic anemia: from lab to bedside","volume":"8","author":"Chaudhary","year":"2014","journal-title":"Asian J. Transfus. Sci"},{"key":"10.1016\/j.cca.2014.12.002_bb0055","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1111\/ped.12153","article-title":"Varied clinical course of aplastic crisis in hereditary spherocytosis","volume":"56","author":"Kataoka","year":"2014","journal-title":"Pediatr. Int."},{"key":"10.1016\/j.cca.2014.12.002_bb0060","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1016\/S0022-3476(05)81081-9","article-title":"Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis","volume":"117","author":"Eber","year":"1990","journal-title":"J. Pediatr."},{"key":"10.1016\/j.cca.2014.12.002_bb0065","doi-asserted-by":"crossref","first-page":"516","DOI":"10.3324\/haematol.2011.052845","article-title":"Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics","volume":"97","author":"Bianchi","year":"2012","journal-title":"Haematologica"},{"key":"10.1016\/j.cca.2014.12.002_bb0070","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1002\/cyto.b.20583","article-title":"Flow cytometric osmotic fragility\u2014an effective screening approach for red cell membranopathies","volume":"80","author":"Warang","year":"2011","journal-title":"Cytometry B Clin. Cytom."},{"key":"10.1016\/j.cca.2014.12.002_bb0075","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1111\/ijlh.12070","article-title":"Hereditary red cell membrane disorders and laboratory diagnostic testing","volume":"35","author":"King","year":"2013","journal-title":"Int. J. Lab. Hematol."},{"key":"10.1016\/j.cca.2014.12.002_bb0080","doi-asserted-by":"crossref","first-page":"1310","DOI":"10.3324\/haematol.12546","article-title":"Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect","volume":"93","author":"Mariani","year":"2008","journal-title":"Haematologica"},{"key":"10.1016\/j.cca.2014.12.002_bb0085","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1056\/NEJM197908233010830","article-title":"Mean cell hemoglobin concentration sometimes useful","volume":"301","author":"Bessman","year":"1979","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.cca.2014.12.002_bb0090","doi-asserted-by":"crossref","first-page":"120","DOI":"10.1542\/peds.2009-0864","article-title":"Hereditary spherocytosis in neonates with hyperbilirubinemia","volume":"125","author":"Christensen","year":"2010","journal-title":"Pediatrics"},{"key":"10.1016\/j.cca.2014.12.002_bb0095","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1007\/s00282-999-0113-8","article-title":"The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis","volume":"41","author":"Chiron","year":"1999","journal-title":"Hematol. Cell Ther."},{"key":"10.1016\/j.cca.2014.12.002_bb0100","doi-asserted-by":"crossref","first-page":"519","DOI":"10.1111\/j.1751-553X.2009.01216.x","article-title":"Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis","volume":"32","author":"Broseus","year":"2010","journal-title":"Int. J. Lab. Hematol."},{"key":"10.1016\/j.cca.2014.12.002_bb0105","doi-asserted-by":"crossref","first-page":"393","DOI":"10.1179\/1607845413Y.0000000149","article-title":"Values of mean cell volume and mean sphered cell volume can differentiate hereditary spherocytosis and thalassemia","volume":"19","author":"Liao","year":"2014","journal-title":"Hematology"}],"container-title":["Clinica Chimica Acta"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0009898114005361?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0009898114005361?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,8,18]],"date-time":"2019-08-18T06:02:45Z","timestamp":1566108165000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0009898114005361"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,2]]},"references-count":21,"alternative-id":["S0009898114005361"],"URL":"https:\/\/doi.org\/10.1016\/j.cca.2014.12.002","relation":{},"ISSN":["0009-8981"],"issn-type":[{"type":"print","value":"0009-8981"}],"subject":[],"published":{"date-parts":[[2015,2]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Misdiagnosis of two cases of hereditary spherocytosis in a family and review of published reports","name":"articletitle","label":"Article Title"},{"value":"Clinica Chimica Acta","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.cca.2014.12.002","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}