The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells.
作者信息
Heimpel Hermann, Kellermann Kerstin, Neuschwander Nadine, Högel Josef, Schwarz Klaus
出版信息
Haematologica. 2010 Jun;95(6):1034-6. doi: 10.3324/haematol.2009.014563. Epub 2010 Apr 26.
Abstract
摘要
相似文献
1
The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells.
Haematologica. 2010 Jun;95(6):1034-6. doi: 10.3324/haematol.2009.014563. Epub 2010 Apr 26.
2
Type I congenital dyserythropoietic anemia (CDA I): ultrastructural findings.
Haematologica. 1983 Jan-Feb;68(1):30-7.
3
Congenital dyserythropoietic anemia type II diagnosed in a 69-year-old patient with iron overload.
Am J Clin Pathol. 1992 Nov;98(5):522-5. doi: 10.1093/ajcp/98.5.522.
4
Internuclear bridging outside of primary myelodysplasia and congenital dyserythropoietic anemia.
Blood. 2018 Jul 12;132(2):236. doi: 10.1182/blood-2018-05-849232.
5
Neonatal manifestations of congenital dyserythropoietic anemia type I.
J Pediatr. 1997 Jul;131(1 Pt 1):95-7. doi: 10.1016/s0022-3476(97)70130-6.
6
Congenital dyserythropoietic anemia type III.
Haematologica. 2000 Jul;85(7):753-7.
7
Erythroblast multinuclearity in bone marrow and spleen. Congenital dyserythropoietic anemia-like abnormalities without functional evidence of dyserythropoiesis.
Arch Pathol Lab Med. 1987 Jun;111(6):536-9.
8
Hairy cell leukemia associated with congenital dyserythropoietic anemia type II (HEMPAS).
Haematologia (Budap). 1994;26(1):39-43.
9
[Elderly dyserythropoietic anemia first diagnosed after presentation of hemorrhagic gastric ulcer].
Rinsho Ketsueki. 1999 Oct;40(10):1074-80.
10
[Extra medullary hematopoiesis associated to congenital dyserythropoietic anemia II in adult].
Ann Biol Clin (Paris). 2012 Mar-Apr;70(2):217-20. doi: 10.1684/abc.2012.0694.
引用本文的文献
1
Congenital Dyserythropoietic Anaemia Type II with SEC23B Mutation in Adults: A Case Series.
Indian J Hematol Blood Transfus. 2025 Jan;41(1):203-206. doi: 10.1007/s12288-024-01806-x. Epub 2024 Jul 1.
2
Congenital Dyserythropoietic Anemia Type I: A Rare Case Report.
Cureus. 2023 Nov 10;15(11):e48594. doi: 10.7759/cureus.48594. eCollection 2023 Nov.
3
Discovering a novel pathogenic CDAN1 variant using exome sequencing and bioinformatics analysis.
Ann Hematol. 2023 Dec;102(12):3621-3623. doi: 10.1007/s00277-023-05419-8. Epub 2023 Aug 21.
4
Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
Ital J Pediatr. 2023 Jul 16;49(1):84. doi: 10.1186/s13052-023-01493-w.
5
New Cases and Mutations in Gene Causing Congenital Dyserythropoietic Anemia Type II.
Int J Mol Sci. 2023 Jun 9;24(12):9935. doi: 10.3390/ijms24129935.
6
Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.
Indian J Pediatr. 2023 Aug;90(8):840. doi: 10.1007/s12098-023-04662-1. Epub 2023 May 19.
7
Rare congenital Dyserythropoietic anemia of childhood: A case report.
Clin Case Rep. 2023 Feb 15;11(2):e6975. doi: 10.1002/ccr3.6975. eCollection 2023 Feb.
8
Congenital dyserythropoietic anaemia type II in a teenager presenting with severe anaemia.
BMJ Case Rep. 2023 Feb 7;16(2):e251756. doi: 10.1136/bcr-2022-251756.
9
Ultrastructural characteristics of erythroid cells in congenital dyserythropoietic anemia type II, with a focus on peripheral cisternae and double membranes.
Blood Sci. 2022 Oct 10;5(1):25-31. doi: 10.1097/BS9.0000000000000136. eCollection 2023 Jan.
10
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.
Int J Mol Sci. 2022 Jan 24;23(3):1304. doi: 10.3390/ijms23031304.
本文引用的文献
1
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.
Blood. 2006 Jan 1;107(1):334-40. doi: 10.1182/blood-2005-01-0421. Epub 2005 Sep 1.
2
Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation.
Blood. 2003 Dec 15;102(13):4576-81. doi: 10.1182/blood-2003-02-0613. Epub 2003 Aug 21.
3
Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data.
Blood Rev. 1998 Sep;12(3):178-200. doi: 10.1016/s0268-960x(98)90016-9.
4
The bone marrow aspirate of healthy subjects.
Br J Haematol. 1996 Dec;95(3):574-5.
5
The bone marrow aspirate of healthy subjects.
Br J Haematol. 1996 Jul;94(1):206-9. doi: 10.1046/j.1365-2141.1996.d01-1786.x.
6
Genetic disorders of the red cell membrane.
Crit Rev Oncol Hematol. 1995 Jun;19(2):79-110. doi: 10.1016/1040-8428(94)00139-k.
7
Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: a type of congenital dyserythropoietic anaemia.
Br J Haematol. 1969 Jul;17(1):11-26. doi: 10.1111/j.1365-2141.1969.tb05660.x.
8
Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts.
Helv Med Acta. 1968 Mar;34(2):103-15.
9
Electron and light microscopic study of the erythroblasts of patients with congenital dyserythropoietic anemia.
Blood. 1971 Mar;37(3):299-310.
10
Congenital dyserythropoietic anaemia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II, as revealed by two-dimensional polyacrylamide gel electrophoresis.
Br J Haematol. 1977 Feb;35(2):209-15. doi: 10.1111/j.1365-2141.1977.tb00577.x.
Zotero 插件