Literature DB >> 25984425

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.

Chao Wang1, Yazhou Cui2, Yan Li1, Xiao Liu1, Jinxiang Han2.   

Abstract

Epidemiological information of hereditary spherocytosis in China is slight. This systematic review summarizes the number of cases of hereditary spherocytosis reported in China Biology Medicine disc from 1978 to 2013. In total, 2,043 cases were reported in the past 36 years. We describe its distribution from time and space. We also estimate the literature reported prevalence of hereditary spherocytosis by DisMod-II software, overall prevalence in China was estimated to be: 1.27 cases per 100,000 people in males and 1.49 cases per 100,000 people in females. All results suggest a stronger network of diagnosis and treatment including all levels of hospitals should be created to improve healthcare for hereditary spherocytosis and even other rare diseases in the future, meanwhile we can obtain more useful information for orphan drug designation purposes and make public health decisions regarding such diseases through the use of the burden of disease models.

Entities:  

Keywords:  Bibliographic study; China; DisMod-II; Hereditary spherocytosis

Year:  2015        PMID: 25984425      PMCID: PMC4428190          DOI: 10.5582/irdr.2015.01002

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  19 in total

1.  Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases.

Authors:  M P Ricard; F Gilsanz; I Millan
Journal:  Haematologica       Date:  2000-09       Impact factor: 9.941

2.  Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.

Authors:  B Bader-Meunier; F Gauthier; F Archambaud; T Cynober; F Miélot; J P Dommergues; J Warszawski; N Mohandas; G Tchernia
Journal:  Blood       Date:  2001-01-15       Impact factor: 22.113

3.  CDC WONDER: a comprehensive on-line public health information system of the Centers for Disease Control and Prevention.

Authors:  A Friede; J A Reid; H W Ory
Journal:  Am J Public Health       Date:  1993-09       Impact factor: 9.308

4.  Quantifying disability: data, methods and results.

Authors:  C J Murray; A D Lopez
Journal:  Bull World Health Organ       Date:  1994       Impact factor: 9.408

5.  Erythropoiesis: Hereditary Spherocytosis in Greece: Collective Data on a Large Number of Patients.

Authors:  EVANGELOS Premetis; ALEXANDRA Stamoulakatou; DIMITRIS Loukopoulos
Journal:  Hematology       Date:  1999       Impact factor: 2.269

6.  Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.

Authors:  D M Bogusławska; E Heger; A Chorzalska; M Nierzwicka; J Hołojda; A Swiderska; A Straburzyńska; G Paździor; M Langner; A F Sikorski
Journal:  Ann Hematol       Date:  2003-09-27       Impact factor: 3.673

7.  Prevalence of scleroderma in Spain: an approach for estimating rare disease prevalence using a disease model.

Authors:  A Villaverde-Hueso; M Posada de la Paz; M C Martín-Arribas; E Sánchez-Valle; A Ramírez-González; P Biairdi
Journal:  Pharmacoepidemiol Drug Saf       Date:  2008-11       Impact factor: 2.890

8.  Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis.

Authors:  J Yoaly Sánchez-López; Ana L Camacho; Maria Teresa Magaña; Bertha Ibarra; F Javier Perea
Journal:  Blood Cells Mol Dis       Date:  2003 Nov-Dec       Impact factor: 3.039

Review 9.  A systematic review of genetic skeletal disorders reported in Chinese biomedical journals between 1978 and 2012.

Authors:  Yazhou Cui; Heng Zhao; Zhenxing Liu; Chao Liu; Jing Luan; Xiaoyan Zhou; Jinxiang Han
Journal:  Orphanet J Rare Dis       Date:  2012-08-22       Impact factor: 4.123

10.  Estimating the prevalence of breast cancer using a disease model: data problems and trends.

Authors:  Michelle E Kruijshaar; Jan J Barendregt; Lonneke V Van De Poll-Franse
Journal:  Popul Health Metr       Date:  2003-04-14
View more
  14 in total

1.  Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing.

Authors:  Li Qin; Yanbo Nie; Hong Zhang; Long Chen; Donglei Zhang; Yani Lin; Kun Ru
Journal:  J Hum Genet       Date:  2020-01-24       Impact factor: 3.172

2.  Novel hereditary spherocytosis-associated splice site mutation in the ANK1 gene caused by parental gonosomal mosaicism.

Authors:  Xiong Wang; Na Shen; Ming Huang; Yanjun Lu; Qun Hu
Journal:  Haematologica       Date:  2018-02-15       Impact factor: 9.941

3.  Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.

Authors:  Lili Hao; Shanshan Li; Duan Ma; Shiyu Chen; Bowen Zhang; Deyong Xiao; Jin Zhang; Nan Jiang; Shayi Jiang; Jing Ma
Journal:  J Cell Mol Med       Date:  2019-04-23       Impact factor: 5.310

4.  A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.

Authors:  Shan Li; Ping Guo; Leyuan Mi; Xiaojing Chai; Kewang Xi; Ting Liu; Li Lu; Juan Li
Journal:  Ann Hematol       Date:  2022-01-31       Impact factor: 3.673

5.  Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis.

Authors:  Jun Xue; Qing He; Xiaojing Xie; Ailing Su; Shibin Cao
Journal:  Ann Transl Med       Date:  2019-10

6.  Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis.

Authors:  Fei Xie; Lei Lei; Bin Cai; Lu Gan; Yu Gao; Xiaoying Liu; Lin Zhou; Jinjin Jiang
Journal:  Mol Genet Genomic Med       Date:  2021-02-23       Impact factor: 2.183

7.  Identification of a novel de novo ANK1 R1426* nonsense mutation in a Chinese family with hereditary spherocytosis by NGS.

Authors:  Xiong Wang; Bin Yi; Ketao Mu; Na Shen; Yaowu Zhu; Qun Hu; Yanjun Lu
Journal:  Oncotarget       Date:  2017-05-27

8.  Targeted next-generation sequencing identifies a novel nonsense mutation in SPTB for hereditary spherocytosis: A case report of a Korean family.

Authors:  Soyoung Shin; Woori Jang; Myungshin Kim; Yonggoo Kim; Suk Young Park; Joonhong Park; Young Jun Yang
Journal:  Medicine (Baltimore)       Date:  2018-01       Impact factor: 1.889

9.  Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report.

Authors:  Jun-Fang Wang; Li Ma; Xiao-Hui Gong; Cheng Cai; Jing-Jing Sun
Journal:  World J Clin Cases       Date:  2021-07-06       Impact factor: 1.337

10.  An ANK1 IVS3-2A>C mutation causes exon 4 skipping in two patients from a Chinese family with hereditary spherocytosis.

Authors:  Xiong Wang; Liyan Mao; Na Shen; Jing Peng; Yaowu Zhu; Qun Hu; Yanjun Lu
Journal:  Oncotarget       Date:  2017-12-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.