Literature DB >> 20712767

Thalassemia as a global health problem: recent progress toward its control in the developing countries.

D J Weatherall1.   

Abstract

The thalassemias, together with sickle cell anemia and its variants, are by far the most common monogenic diseases. They occur at their highest frequency in countries of the developing world where their control and management is hampered by a lack of knowledge of their true prevalence, adequate services for their management and control, and support by their governments and international health agencies. However, there has been some progress recently in addressing these problems and there are several ways in which the lot of children with thalassemia in poor countries could be improved in the future. Over the last 20 years there has been considerable improvement in the control and management of the thalassemias in the richer countries of the world. Unfortunately, however, this is not the case for many of the developing countries, where there have been few improvements in the control of the numbers of births of babies with thalassemia or in the care of thalassemic children since the frequency of the problem started to become evident in the 1960s. Here, I will try to assess the current situation in these countries and examine some of the potential approaches for improving the current situation.

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Year:  2010        PMID: 20712767     DOI: 10.1111/j.1749-6632.2010.05546.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  38 in total

1.  Comparative Proteome-Wide Analysis of Bone Marrow Microenvironment of β-Thalassemia/Hemoglobin E.

Authors:  Saranyoo Ponnikorn; Rungrawee Mongkolrob; Suwit Klongthalay; Sittiruk Roytrakul; Kitima Srisanga; Sumalee Tungpradabkul; Suradej Hongeng
Journal:  Proteomes       Date:  2019-02-23

2.  Red blood cell indices and prevalence of hemoglobinopathies and glucose 6 phosphate dehydrogenase deficiencies in male Tanzanian residents of Dar es Salaam.

Authors:  Solomon Mwakasungula; Tobias Schindler; Said Jongo; Elena Moreno; Kasimu Kamaka; Mgeni Mohammed; Selina Joseph; Ramla Rashid; Thabit Athuman; Anneth Mwasi Tumbo; Ali Hamad; Omar Lweno; Marcel Tanner; Seif Shekalaghe; Claudia A Daubenberger
Journal:  Int J Mol Epidemiol Genet       Date:  2014-12-15

Review 3.  The inherited diseases of hemoglobin are an emerging global health burden.

Authors:  David J Weatherall
Journal:  Blood       Date:  2010-03-16       Impact factor: 22.113

4.  Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel.

Authors:  Emanuele Angelucci; Susanne Matthes-Martin; Donatella Baronciani; Françoise Bernaudin; Sonia Bonanomi; Maria Domenica Cappellini; Jean-Hugues Dalle; Paolo Di Bartolomeo; Cristina Díaz de Heredia; Roswitha Dickerhoff; Claudio Giardini; Eliane Gluckman; Ayad Achmed Hussein; Naynesh Kamani; Milen Minkov; Franco Locatelli; Vanderson Rocha; Petr Sedlacek; Frans Smiers; Isabelle Thuret; Isaac Yaniv; Marina Cavazzana; Christina Peters
Journal:  Haematologica       Date:  2014-05       Impact factor: 9.941

5.  Managing the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore.

Authors:  Neha Kumar; Erin Turbitt; Barbara B Biesecker; Ilana M Miller; Breana Cham; Katherine C Smith; Rajiv N Rimal
Journal:  Am J Med Genet A       Date:  2019-03-01       Impact factor: 2.802

6.  Therapeutic effects of induced pluripotent stem cells in chimeric mice with β-thalassemia.

Authors:  Guanheng Yang; Wansheng Shi; Xingyin Hu; Jingzhi Zhang; Zhijuan Gong; Xinbing Guo; Zhaorui Ren; Fanyi Zeng
Journal:  Haematologica       Date:  2014-05-09       Impact factor: 9.941

Review 7.  The prevention of thalassemia.

Authors:  Antonio Cao; Yuet Wai Kan
Journal:  Cold Spring Harb Perspect Med       Date:  2013-02-01       Impact factor: 6.915

8.  First report of pediatric hematopoietic stem cell transplantation activities in the eastern mediterranean region from 1984 to 2011: on behalf of the pediatric cancer working committee of the eastern mediterranean blood and marrow transplantation group.

Authors:  A A Hussein; A A Hamidieh; A Elhaddad; M Ramzi; T B Othman; F Hussain; D Dennison; P Ahmed; M Abboud; A Al-Ahmari; A Wahadneh; J Fathy; M-A Bekadja; S Al-Kindi; S Benchekroun; A Ibrahim; M Behfar; M Samra; S Ladeb; S Adil; H El-Solh; M Ayas; M Aljurf; A Ghavamzadeh; A Al-Seraihy
Journal:  Bone Marrow Transplant       Date:  2016-09-12       Impact factor: 5.483

Review 9.  World distribution, population genetics, and health burden of the hemoglobinopathies.

Authors:  Thomas N Williams; David J Weatherall
Journal:  Cold Spring Harb Perspect Med       Date:  2012-09-01       Impact factor: 6.915

10.  Feasibility of and barriers to thalassemia screening in migrant populations: a cross-sectional study of Myanmar and Cambodian migrants in Thailand.

Authors:  Julia Z Xu; Wilaslak Tanongsaksakul; Thidarat Suksangpleng; Supachai Ekwattanakit; Suchada Riolueang; Marilyn J Telen; Vip Viprakasit
Journal:  BMC Public Health       Date:  2021-06-21       Impact factor: 3.295

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