Literature DB >> 18991645

Hemoglobinopathies worldwide: present and future.

David J Weatherall1.   

Abstract

The genetic disorders of hemoglobin, the commonest monogenic diseases, occur at some of their highest frequencies in the developing countries, particularly those of Sub-Saharan Africa and Asia. Although progress towards their control and management continues to be made, the prospects for curing them, apart from marrow transplantation, remain uncertain. In many countries expertise and facilities for their control are extremely limited. Although a great deal can be done to help the situation by developing further North/South and South/South partnerships for disseminating better practice, the major problem for the future lies in the unwillingness of governments and international health agencies to accept that the hemoglobinopathies represent a health burden comparative to that of communicable and other major diseases. However, preliminary analyses suggest that, at least in the case of Asia, this may not be true. Further work of this type, together with more detailed frequency and economic data, is required to provide solid evidence for the health burden posed by the hemoglobin disorders, particularly in the developing world. Unless this is done, the increasingly large populations of patients with these diseases will continue to be neglected.

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Year:  2008        PMID: 18991645     DOI: 10.2174/156652408786241375

Source DB:  PubMed          Journal:  Curr Mol Med        ISSN: 1566-5240            Impact factor:   2.222


  30 in total

1.  Psychosocial burden of sickle cell disease on parents with an affected child in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2013-07-24       Impact factor: 2.537

2.  Frequent red cell transfusions reduced vascular endothelial activation and thrombogenicity in children with sickle cell anemia and high stroke risk.

Authors:  Hyacinth I Hyacinth; Robert J Adams; Jenifer H Voeks; Jacqueline M Hibbert; Beatrice E Gee
Journal:  Am J Hematol       Date:  2013-11-28       Impact factor: 10.047

3.  Hemoglobinopathies: clinical manifestations, diagnosis, and treatment.

Authors:  Elisabeth Kohne
Journal:  Dtsch Arztebl Int       Date:  2011-08-08       Impact factor: 5.594

Review 4.  Clinical manifestations of α-thalassemia.

Authors:  Elliott P Vichinsky
Journal:  Cold Spring Harb Perspect Med       Date:  2013-05-01       Impact factor: 6.915

5.  Intestine-specific Disruption of Hypoxia-inducible Factor (HIF)-2α Improves Anemia in Sickle Cell Disease.

Authors:  Nupur Das; Liwei Xie; Sadeesh K Ramakrishnan; Andrew Campbell; Stefano Rivella; Yatrik M Shah
Journal:  J Biol Chem       Date:  2015-08-19       Impact factor: 5.157

6.  Can Trimodal Distribution of HbS Levels in Sickle Cell Traits Be Used To Predict the Associated Alpha-Thalassemia For Screening Cases in Central India?

Authors:  B M Warpe; A V Shrikhande; S V Poflee
Journal:  Iran J Pathol       Date:  2016

7.  Acceptability of prenatal diagnosis by a sample of parents of sickle cell anemia patients in Cameroon (sub-Saharan Africa).

Authors:  Ambroise Wonkam; Alfred K Njamnshi; Dora Mbanya; Jeanne Ngogang; Caryl Zameyo; Fru F Angwafo
Journal:  J Genet Couns       Date:  2011-05-21       Impact factor: 2.537

8.  β-Globin chain abnormalities with coexisting α-thalassemia mutations.

Authors:  Birol Guvenc; Abdullah Canataroglu; Cagatay Unsal; Sule Menziletoglu Yildiz; Ferda Tekin Turhan; Sevcan Tug Bozdogan; Suleyman Dincer; Hakan Erkman
Journal:  Arch Med Sci       Date:  2012-05-29       Impact factor: 3.318

Review 9.  Genome-based therapeutic interventions for β-type hemoglobinopathies.

Authors:  Kariofyllis Karamperis; Maria T Tsoumpeli; Fotios Kounelis; Maria Koromina; Christina Mitropoulou; Catia Moutinho; George P Patrinos
Journal:  Hum Genomics       Date:  2021-06-05       Impact factor: 4.639

10.  Efficient detection of Mediterranean β-thalassemia mutations by multiplex single-nucleotide primer extension.

Authors:  Biljana Atanasovska; Georgi Bozhinovski; Dijana Plaseska-Karanfilska; Lyubomira Chakalova
Journal:  PLoS One       Date:  2012-10-26       Impact factor: 3.240

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