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Quoted phrase not found in phrase index: "Congenital dyserythropoietic anemia type 4"
Page 1
Hematopoietic Cell Transplantation for Congenital Dyserythropoietic Anemia: A Report from the Pediatric Transplant and Cellular Therapy Consortium.
Rangarajan HG, Stanek JR, Abdel-Azim H, Modi A, Haight A, McKinney CM, McKeone DJ, Buchbinder DK, Katsanis E, Abusin GA, Ahmed I, Law J, Silva JG, Mallhi KK, Burroughs LM, Shah N, Shaw PJ, Greiner R, Shenoy S, Pulsipher MA, Abu-Arja R. Rangarajan HG, et al. Transplant Cell Ther. 2022 Jun;28(6):329.e1-329.e9. doi: 10.1016/j.jtct.2022.03.007. Epub 2022 Mar 11. Transplant Cell Ther. 2022. PMID: 35288346 Free article.
Hematopoietic cell transplantation (HCT) is the sole curative option for congenital dyserythropoietic anemia (CDA), a rare type of hemolytic anemia characterized by anemia, ineffective erythropoiesis, and secondary hemochromatosis. ...Eig …
Hematopoietic cell transplantation (HCT) is the sole curative option for congenital dyserythropoietic anemia (CDA), a r …
Congenital Hemolytic Anemias: Is There a Role for the Immune System?
Zaninoni A, Fermo E, Vercellati C, Marcello AP, Barcellini W, Bianchi P. Zaninoni A, et al. Front Immunol. 2020 Jun 23;11:1309. doi: 10.3389/fimmu.2020.01309. eCollection 2020. Front Immunol. 2020. PMID: 32655575 Free PMC article. Review.
They are characterized by variable degree of anemia, chronic extravascular hemolysis, reduced erythrocyte life span, splenomegaly, jaundice, biliary lithiasis, and iron overload. ...Median Hb increase is 3 g/dL in HS, 1.6-1.8 g/dL in pyruvate kinase deficiency (PKD), and 1 …
They are characterized by variable degree of anemia, chronic extravascular hemolysis, reduced erythrocyte life span, splenomegaly, ja …
Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.
Resnitzky P, Shaft D, Shalev H, Kapelushnik J, Dgany O, Krasnov T, Tamary H. Resnitzky P, et al. Eur J Haematol. 2017 Oct;99(4):366-371. doi: 10.1111/ejh.12931. Epub 2017 Aug 29. Eur J Haematol. 2017. PMID: 28755517
INTRODUCTION: Congenital dyserythropoietic anemias are rare blood disorders characterized by congenital anemia and a wide range of morphological and functional abnormalities of erythroid precursors. OBJECTIVES: To analyze the relative frequency of both …
INTRODUCTION: Congenital dyserythropoietic anemias are rare blood disorders characterized by congenital anemia a …
Managing the Unusual Causes of Fetal Anemia.
Maisonneuve E, Ben M'Barek I, Leblanc T, Da Costa L, Friszer S, Pernot F, Thomas P, Castaigne V, Toly N'Dour C, Mailloux A, Cortey A, Jouannic JM. Maisonneuve E, et al. Fetal Diagn Ther. 2020;47(2):156-164. doi: 10.1159/000501554. Epub 2019 Sep 10. Fetal Diagn Ther. 2020. PMID: 31505487
The fetuses received between 1 and 6 IUT (39% received at least 2 IUT). The definitive etiologies for central anemia were: congenital syphilis, neonatal poikilocytosis, type II congenital dyserythropoietic anemia (CDA), and neonatal hemoc …
The fetuses received between 1 and 6 IUT (39% received at least 2 IUT). The definitive etiologies for central anemia were: congeni …
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children.
Bader-Meunier B, Leverger G, Tchernia G, Schischmanoff O, Cynober T, Bernaudin F, Leblanc T, Munzer M, Roda L, Soler C, Thuret I, Delaunay J. Bader-Meunier B, et al. J Pediatr Hematol Oncol. 2005 Aug;27(8):416-9. doi: 10.1097/01.mph.0000175406.42427.c9. J Pediatr Hematol Oncol. 2005. PMID: 16096522
Congenital dyserythropoietic anemia type I (CDA I) is a rare disorder of erythropoiesis. ...It should be sought in patients with unexplained chronic anemia, especially when associated with neonatal manifestations, jaundice, splenomegaly, subnorm …
Congenital dyserythropoietic anemia type I (CDA I) is a rare disorder of erythropoiesis. ...It should be sought …
Pregnancy outcome in congenital dyserythropoietic anemia type I.
Shalev H, Avraham GP, Hershkovitz R, Levy A, Sheiner E, Levi I, Tamary H. Shalev H, et al. Eur J Haematol. 2008 Oct;81(4):317-21. doi: 10.1111/j.1600-0609.2008.01109.x. Epub 2008 Jun 28. Eur J Haematol. 2008. PMID: 18573172
OBJECTIVES: Congenital dyserythropoietic anemia type I (CDA I) is a rare inherited disease characterized by moderate to severe macrocytic anemia and abnormal erythroid precursors with nuclear chromatin bridges and spongy heterochromatin. ...The …
OBJECTIVES: Congenital dyserythropoietic anemia type I (CDA I) is a rare inherited disease characterized by mode …
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.
Heimpel H, Schwarz K, Ebnöther M, Goede JS, Heydrich D, Kamp T, Plaumann L, Rath B, Roessler J, Schildknecht O, Schmid M, Wuillemin W, Einsiedler B, Leichtle R, Tamary H, Kohne E. Heimpel H, et al. Blood. 2006 Jan 1;107(1):334-40. doi: 10.1182/blood-2005-01-0421. Epub 2005 Sep 1. Blood. 2006. PMID: 16141353 Free article.
Congenital dyserythropoietic anemia type I (CDA I) is a rare autosomal recessive disorder with ineffective erythropoiesis and iron overloading. ...Twenty-one patients with a confirmed diagnosis of CDA I exhibited chronic macrocytic anemia of var …
Congenital dyserythropoietic anemia type I (CDA I) is a rare autosomal recessive disorder with ineffective eryth …
Natural history of congenital dyserythropoietic anemia type II.
Iolascon A, Delaunay J, Wickramasinghe SN, Perrotta S, Gigante M, Camaschella C. Iolascon A, et al. Blood. 2001 Aug 15;98(4):1258-60. doi: 10.1182/blood.v98.4.1258. Blood. 2001. PMID: 11493480 Free article.
Congenital dyserythropoietic anemia type II (CDA-II) is an autosomal recessive disease characterized by anemia, jaundice, splenomegaly, and erythroblast multinuclearity. ...Retrospective data were obtained using an appropriate questionnaire. The …
Congenital dyserythropoietic anemia type II (CDA-II) is an autosomal recessive disease characterized by anemi …
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).
Perrotta S, del Giudice EM, Carbone R, Servedio V, Schettini F Jr, Nobili B, Iolascon A. Perrotta S, et al. J Pediatr. 2000 Apr;136(4):556-9. doi: 10.1016/s0022-3476(00)90026-x. J Pediatr. 2000. PMID: 10753261 Review.
The molecular basis for the considerable variation of serum bilirubin levels and the incidence of gallstone formation in patients with congenital dyserythropoietic anemia (CDA) type II are unknown. We show that the combined effect of an increased bilir …
The molecular basis for the considerable variation of serum bilirubin levels and the incidence of gallstone formation in patients with co …
A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country.
Aly NH, Elalfy MS, Elhabashy SA, Mowafy NM, Russo R, Andolfo I, Iolascon A, Ragab IA. Aly NH, et al. Blood Cells Mol Dis. 2023 Nov;103:102779. doi: 10.1016/j.bcmd.2023.102779. Epub 2023 Jul 16. Blood Cells Mol Dis. 2023. PMID: 37558589
BACKGROUND: Reaching a precise diagnosis in rare inherited anemia is extremely difficult and challenging, especially in areas with limited use of genetic studies, which makes undiagnosed anemia a unique clinical entity in tertiary hematology centers. ...In the normo …
BACKGROUND: Reaching a precise diagnosis in rare inherited anemia is extremely difficult and challenging, especially in areas with li …
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