Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference20 articles.
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2. Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer
3. A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model
4. Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis
5. Delhommeau F, Cynober T, Schischmanoff PO, Rohrlich P, Delaunay J, Mohandas N, Tchernia G. Natural history of hereditary spherocytosis during the first year of life. Blood 2000; 95: 393-397
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Case report: Genetic analysis of a novel intronic inversion variant in the SPTB gene associated with hereditary spherocytosis;Frontiers in Genetics;2023-12-04
2. Reverse complete heart block using transcutaneous pacing and repeated plasmapheresis in a neonate with lupus: a case report;Pediatric Rheumatology;2023-11-09
3. Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis;Frontiers in Genetics;2023-02-01
4. A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis;Acta Haematologica;2022
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