Literature DB >> 1659863

Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions.

S N Wickramasinghe1, N Illum, P D Wimberley.   

Abstract

A hitherto undescribed form of congenital dyserythropoietic anaemia is reported. The patient was severely anaemic and hydropic at birth and is now 8 years old. She has a moderate normochromic normocytic anaemia. HbF level of 50%, reticulocyte count of 5-12% and hyperbilirubinaemia. Bone marrow smears showed intense normoblastic erythroid hyperplasia with morphological evidence of dyserythropoiesis; the most common dysplastic features were basophilic stippling of polychromatic erythroblasts and erythrocytes and marked abnormalities of nuclear shape in polychromatic erythroblasts. Electron microscope studies showed that some polychromatic erythroblasts and several erythrocytes contained inclusions which were rounded, elongated or irregular in outline or were doughnut-shaped. These inclusions consisted of compact masses of tubules and saccules which may represent smooth endoplastic reticulum together with Golgi cisternae. The ultrastructural studies also revealed peculiar membrane-bound cylindrical structures in a rare late erythroblast, and phagocytosed erythroblasts within some macrophages. The technique of combined Feulgen microspectrophotometry and 3H-thymidine autoradiography demonstrated a pile-up of early polychromatic erythroblasts in the G1 and G2 phases of the cell cycle, indicating a prolongation of, or an arrest at, these phases. Furthermore, nearly a quarter of all erythroblasts failed to incorporate 3H-leucine into protein. Thus the anaemia appeared to be due to a combination of disordered erythroblast function, increased ineffectiveness of erythropoiesis and peripheral haemolysis. The primary defect may be an excessive synthesis or impaired degradation of intracytoplasmic membranes.

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Year:  1991        PMID: 1659863     DOI: 10.1111/j.1365-2141.1991.tb04541.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  9 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

Review 3.  Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm.

Authors:  Julie A Jaffray; W Beau Mitchell; Merlin Nithya Gnanapragasam; Surya V Seshan; Xinhuo Guo; Connie M Westhoff; James J Bieker; Deepa Manwani
Journal:  Blood Cells Mol Dis       Date:  2013-03-20       Impact factor: 3.039

4.  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

5.  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

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.  Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors.

Authors:  Melissa D Ilsley; Stephen Huang; Graham W Magor; Michael J Landsberg; Kevin R Gillinder; Andrew C Perkins
Journal:  BMC Genomics       Date:  2019-05-24       Impact factor: 3.969

8.  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

Review 9.  Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.

Authors:  Achille Iolascon; Hermann Heimpel; Anders Wahlin; Hannah Tamary
Journal:  Blood       Date:  2013-08-12       Impact factor: 22.113

  9 in total

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