Literature DB >> 20665989

Frequency of congenital dyserythropoietic anemias in Europe.

Hermann Heimpel1, Andreas Matuschek, Momin Ahmed, Brigitte Bader-Meunier, Adriana Colita, Jean Delaunay, Loic Garcon, Florinda Gilsanz, Jeroen Goede, Josef Högel, Elisabeth Kohne, Rosi Leichtle, Juan Munoz, Silverio Perrotta, Carlo Piscopo, Raffaele Renella, Klaus Schwarz, Gabriela Smolenska-Sym, Sunitha Wickramasinghe, Alberto Zanella, Achille Iolascon.   

Abstract

Congenital dyserythropoietic anemias (CDAs) are rare hereditary disorders characterized by ineffective erythropoiesis and striking abnormalities of erythroblast morphology. The mutated genes are known for the most frequent types, CDA I and II, but data about their frequency do not exist. The objective of this retrospective study was to estimate the frequency of CDA I and II, based on all cases reported in the last 42 yr in publications and identified registries or surveys. Reports were collected of 124 and 377 confirmed cases of CDA I and CDA II cases, respectively. The cumulated incidence of both types combined varied widely between European regions, with minimal values of 0.08 cases/million in Scandinavia and 2.60 cases/million in Italy. CDA II is more frequent than CDA I, with an overall ratio of approximately 3.2, but the ratio also varied between different regions. The most likely explanations for the differences are both differences in the availability of advanced diagnostic procedures and different levels of the awareness for the diagnosis of the CDAs. The estimations reported here are most probably below the true incidence rates, because of failure to make the correct diagnosis and to underreporting. Limited data do not suggest differing levels of risk in identified ethnic groups.

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Year:  2010        PMID: 20665989

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  13 in total

1.  KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome.

Authors:  Graham W Magor; Michael R Tallack; Kevin R Gillinder; Charles C Bell; Naomi McCallum; Bronwyn Williams; Andrew C Perkins
Journal:  Blood       Date:  2015-02-27       Impact factor: 22.113

Review 2.  Congenital dyserythropoietic anaemias: new acquisitions.

Authors:  Achille Iolascon; Roberta Russo; Maria Rosaria Esposito; Carmelo Piscopo; Roberta Asci; Luigia De Falco; Francesca Di Noce
Journal:  Blood Transfus       Date:  2010-12-13       Impact factor: 3.443

3.  Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II.

Authors:  Shanshan Chen; Ziwen Guo; Yongbin Ye; Shanhong Yang; Guinian Huang
Journal:  Int J Hematol       Date:  2021-04-29       Impact factor: 2.490

4.  [Whole exome sequencing analysis of compound heterozygous variants of CDAN1 gene in a Chinese family with non-immune hydrops fetalis].

Authors:  Y Wang; Q Li; X Sun; S Li; J He; M Zhang; L Huang; W He
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2021-12-20

Review 5.  The congenital dyserythropoieitic anemias: genetics and pathophysiology.

Authors:  Richard King; Patrick J Gallagher; Rami Khoriaty
Journal:  Curr Opin Hematol       Date:  2021-12-24       Impact factor: 3.218

6.  Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene.

Authors:  Francesca Punzo; Aida M Bertoli-Avella; Saverio Scianguetta; Fulvio Della Ragione; Maddalena Casale; Luisa Ronzoni; Maria D Cappellini; Gianluca Forni; Ben A Oostra; Silverio Perrotta
Journal:  Orphanet J Rare Dis       Date:  2011-12-30       Impact factor: 4.123

7.  Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population.

Authors:  Roberta Russo; Antonella Gambale; Maria Rosaria Esposito; Maria Luisa Serra; Annaelena Troiano; Ilaria De Maggio; Mario Capasso; Lucio Luzzatto; Jean Delaunay; Hannah Tamary; Achille Iolascon
Journal:  Am J Hematol       Date:  2011-09       Impact factor: 10.047

8.  A case of congenital dyserythropoietic anemia type IV.

Authors:  Silvia de-la-Iglesia-Iñigo; María-Isabel Moreno-Carralero; Angelina Lemes-Castellano; Teresa Molero-Labarta; Manuel Méndez; María-José Morán-Jiménez
Journal:  Clin Case Rep       Date:  2017-01-28

Review 9.  Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach.

Authors:  Achille Iolascon; Maria Rosaria Esposito; Roberta Russo
Journal:  Haematologica       Date:  2012-10-12       Impact factor: 9.941

10.  Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.

Authors:  Christian Babbs; Nigel A Roberts; Luis Sanchez-Pulido; Simon J McGowan; Momin R Ahmed; Jill M Brown; Mohamed A Sabry; David R Bentley; Gil A McVean; Peter Donnelly; Opher Gileadi; Chris P Ponting; Douglas R Higgs; Veronica J Buckle
Journal:  Haematologica       Date:  2013-05-28       Impact factor: 9.941

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