Literature DB >> 7680924

Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia.

W Tang1, S P Cai, B Eng, M C Poon, J S Waye, N Illum, D H Chui.   

Abstract

A 10-year-old Danish girl with congenital anemia is described. At birth, she had severe anemia and erythroblastosis and was transfused a number of times during the first year. The need for transfusions has since declined steadily. Her reticulocyte counts varied between 2% and 15%, and her bone marrow aspirate showed some dyserythropoietic features. Her hemoglobin F level was consistently elevated, up to as much as 41%. Her erythrocytes had a normal level of I antigen but an undetectable level of i antigen. Moreover, embryonic zeta-globin and epsilon-globin chains were present in some of her circulating erythrocytes. These findings may represent the manifestations of a new variant of congenital anemia.

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Year:  1993        PMID: 7680924

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  7 in total

1.  Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor.

Authors:  Miroslawa Siatecka; Kenneth E Sahr; Sabra G Andersen; Mihaly Mezei; James J Bieker; Luanne L Peters
Journal:  Proc Natl Acad Sci U S A       Date:  2010-08-09       Impact factor: 11.205

2.  A Krüppel-like factor 1 (KLF1) Mutation Associated with Severe Congenital Dyserythropoietic Anemia Alters Its DNA-Binding Specificity.

Authors:  Klaudia Kulczynska; James J Bieker; Miroslawa Siatecka
Journal:  Mol Cell Biol       Date:  2020-02-12       Impact factor: 4.272

3.  Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.

Authors:  P Agre; B L Smith; R Baumgarten; G M Preston; E Pressman; P Wilson; N Illum; D J Anstee; M B Lande; M L Zeidel
Journal:  J Clin Invest       Date:  1994-09       Impact factor: 14.808

4.  A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.

Authors:  Lionel Arnaud; Carole Saison; Virginie Helias; Nicole Lucien; Dominique Steschenko; Marie-Catherine Giarratana; Claude Prehu; Bernard Foliguet; Lory Montout; Alexandre G de Brevern; Alain Francina; Pierre Ripoche; Odile Fenneteau; Lydie Da Costa; Thierry Peyrard; Gail Coghlan; Niels Illum; Henrik Birgens; Hannah Tamary; Achille Iolascon; Jean Delaunay; Gil Tchernia; Jean-Pierre Cartron
Journal:  Am J Hum Genet       Date:  2010-11-04       Impact factor: 11.025

5.  Structural determinants of human ζ-globin mRNA stability.

Authors:  Zhenning He; Decheng Song; Sebastiaan van Zalen; J Eric Russell
Journal:  J Hematol Oncol       Date:  2014-04-21       Impact factor: 17.388

6.  KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity.

Authors:  Yaddanapudi Ravindranath; Robert M Johnson; Gerard Goyette; Steven Buck; Manisha Gadgeel; Patrick G Gallagher
Journal:  J Pediatr Hematol Oncol       Date:  2018-08       Impact factor: 1.289

7.  Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient.

Authors:  Lilian Varricchio; Antanas Planutis; Deepa Manwani; Julie Jaffray; W Beau Mitchell; Anna Rita Migliaccio; James J Bieker
Journal:  Haematologica       Date:  2019-03-14       Impact factor: 9.941

  7 in total

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