Congenital dyserythropoietic anemia in China: a case report from two families and a review-Reference-Cited by-同舟云学术

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Congenital dyserythropoietic anemia in China: a case report from two families and a review

Published:2013-11-07 Issue:5 Volume:93 Page:773-777
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Ru Yongxin,Liu Gang,Bai Jie,Dong Shuxu,Nie Neng,Zhang Huamei,Zhao Shixuan,Zheng Yizhou,Zhu Xiaofan,Nie Guangjun,Zhang Fengkui,Eyden Brian

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-013-1933-8.pdf

Reference20 articles.

1. Iolascon A, Esposito MR, Russo R (2012) Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach. Haematologica 97:1786–1794

2. Liljeholm M, Irvine AF, Vikberg AL et al (2013) Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23. Blood 6(121):4791–4799

3. Heimpel H, Matuschek A, Ahmed M et al (2010) Frequency of congenital dyserythropoietic anemias in Europe. Eur J Haematol 85:20–25

4. Singh KI, Shartsho JT, Singh WR et al (2007) Congenital dyserythropoietic anemia type II—a case report of two siblings in a family. Indian J Hematol Blood Transfus 23:116–118

5. Kawabata H, Doisaki S, Okamoto A et al (2012) A case of congenital dyserythropoietic anemia type 1 in a Japanese adult with a CDAN1 gene mutation and an inappropriately low serum hepcidin-25 level. Intern Med 51:917–920

Cited by 10 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. Ultrastructural characteristics of erythroid cells in congenital dyserythropoietic anemia type II, with a focus on peripheral cisternae and double membranes;Blood Science;2022-10-10

2. Congenital dyserythropoiesis anemia type Ia with a novel CDAN1 mutation diagnosed by whole exome sequencing;Molecular Genetics & Genomic Medicine;2020-03-11

3. Fetal-onset Congenital Dyserythropoietic Anemia Type 1 due to a Novel Mutation With Severe Iron Overload and Severe Cholestatic Liver Disease;Journal of Pediatric Hematology/Oncology;2019-01

4. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia;International Journal of Hematology;2018-06-23

5. A novel anemia associated with membranous cytoplasm degeneration in 16 patients: an ultrastructural study;Ultrastructural Pathology;2018-06-18

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