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Artykuł oryginalny
Frequency and predictors of blood transfusion and splenectomy in pediatric hereditary spherocytosis – a single-center retrospective analysis
Aleksandra Osińska
1
,
Marta Druszcz
1
,
Maksymilian Seweryn
1
,
Natalia Czarnecka
1
,
Aleksandra Kozińska
1
,
Dawid Grela
1
,
Monika Lejman
2
,
Małgorzata Mitura-Lesiuk
3
,
Joanna Zawitkowska
3
Pediatr Pol 2025; 100 (4)
Data publikacji online: 2025/11/24
Plik artykułu:
- Frequency and predictors.pdf
[0.18 MB]
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1. Cheng J, Zhang L, Jiang J. Clinical characteristics of hereditary spherocytosis with red blood cell membrane protein gene variants. Front Pediatr 2025; 13: 1523288. 2.
Turpaev K, Bovt E, Shakhidzhanov S, Sinauridze E, Smetanina N, Koleva L, et al. An overview of hereditary spherocytosis and the curative effects of splenectomy. Front Physiol 2025; 16: 1497588. 3.
Ramjist JK, Dubljevic T, Langer JC, Grace RF, Heeney MM, Oni MO, et al. Correlation of genetic mutation with outcomes in children with hereditary spherocytosis undergoing partial splenectomy: a multicentre study. J Pediatr Surg 2025; 60: 162229. 4.
Guizzetti L. Temporal trends of splenectomy in pediatric hospitalizations with hereditary spherocytosis from 2000 to 2019: a national survey. Pediatr Blood Cancer 2024; 71: e30869. 5.
Cheng CK, Chan LC, Tang MH, Jiang W, Xu J, Rao Y, et al. Clinical features and molecular genetics of hereditary spherocytosis in Chinese children. Haematologica 2005; 90: 784-785. 6.
Ang SH, Lam JCM. Hereditary spherocytosis in an Asian children’s hospital. HK J Paediatr (New Series) 2022; 27: 113-117. 7.
Celik SS , Genc DB, Yildirmak ZY. Clinical characteristics and treatment outcome of hereditary spherocytosis: a single center’s experience. Sisli Etfal Hasta Tip Bul 2023; 57: 531-535. 8.
Kiliç MA, Özdemir GN, Tahtakesen TN, Gökçe M, Uysalol EP, Bayram C, et al. Clinical features and outcome of children with hereditary spherocytosis. J Pediatr Hematol Oncol 2022; 44: e306-e309. 9.
Tole S, Dhir P, Pugi J, Drury LJ, Butchart S, Fantauzzi M, et al. Genotype-phenotype correlation in children with hereditary spherocytosis. Br J Hematol 2020; 19: 486-496. 10.
Van Vuren A, van der Zwaag B, Huisjes R, Lak N, Bierings M, Gerritsen E, et al. The complexity of genotype-phenotype correlations in hereditary spherocytosis: a cohort of 95 patients: genotype-phenotype correlation in hereditary spherocytosis. Hemasphere 2019; 3: e276. 11.
Wu C, Xiong T, Xu Z, Zhan C, Chen F, Ye Y, et al. Preliminary study on the clinical and genetic characteristics of hereditary spherocytosis in 15 Chinese children. Front Genet 2021; 12: 652376. 12.
Wu C, Yan Y, Xiong T, Jiang W, Xu J, Rao Y, et al. Clinical and genetic characteristics of Chinese pediatric and adult patients with hereditary spherocytosis. Orphanet J Rare Dis 2024; 19: 278. 13.
Tang X, Xue J, Zhang J, Zhou J. The efficacy of partial versus total splenectomy in the treatment of hereditary spherocytosis in children: a systematic review and meta-analysis. Pediatr Surg Int 2024; 40: 280. 14.
Häuser F, Rossmann H, Adenaeuer A, Shrestha A, Marandiuc D, Paret C, et al. Hereditary spherocytosis: can next-generation sequencing of the five most frequently affected genes replace time-consuming functional investigations? Int J Mol Sci 2023; 24: 17021. 15.
Wang X, Zhang A, Huang M, Chen L, Hu Q, Lu Y, et al. Genetic and clinical characteristics of patients with hereditary spherocytosis in hubei province of China. Front Genet 202; 11: 953. 16.
Zamora EA, Schaefer CA. Hereditary spherocytosis. StatPearls, StatPearls. Available from: https://pubmed.ncbi.nlm.nih.gov/30969619/ (accessed: 04. 06.2023). 17.
Qin L, Nie Y, Zhang H, Chen L, Zhang D, Lin Y, et al. Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing. J Hum Genet 2020; 65: 427-434. 18.
Wang Y, Liu T, Jia C, Xiao L, Wang W, Zhang Y, et al. A novel variant in the SPTB gene underlying hereditary spherocytosis and a literature review of previous variants. BMC Med Genom 2024; 17: 206.
Copyright: © 2025 Polish Society of Paediatrics. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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