Literature DB >> 15358726

Thalassemia in Sri Lanka: a progress report.

Anuja Premawardhena1, Shanthimala De Silva, Mahinda Arambepola, Nancy Olivieri, Laura Merson, Julia Muraco, Angela Allen, Christopher Fisher, Timothy Peto, Elliot Vichinsky, David Weatherall.   

Abstract

The thalassemias pose an increasing burden for health-care services in many Asian countries. In order to conserve rare resources, it is essential to determine the reasons for the remarkable phenotypic heterogeneity and natural history of these disorders so that the most cost-effective methods for their control and management can be established. A long-term observational study of patients with different forms of thalassemia in Sri Lanka suggests that in addition to the well-defined primary, secondary and tertiary genetic modifiers, environmental factors, particularly malaria, and variation in the ability to adapt to the profound anaemia which characterizes these conditions, may play a significant role in determining their clinical severity. These findings may have important implications for the control and management of thalassemia in Asian populations.

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Year:  2004        PMID: 15358726     DOI: 10.1093/hmg/ddh250

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  8 in total

1.  Descriptive profile of β-thalassemia mutations in West Bengal population: a hospital-based study.

Authors:  Deboshree M Bhattacharyya; Ashis Mukhopadhyay; Jayasri Basak
Journal:  Int J Hematol       Date:  2014-02-01       Impact factor: 2.490

2.  β-Thalassaemia and its Co-existence with Haemoglobin E and Haemoglobin S in Upper Assam Region of North Eastern India: A Hospital Based Study.

Authors:  Anju Barhai Teli; Rumi Deori; Sidhartha Protim Saikia; Kalyani Pathak; Rita Panyang; Rashmi Rajkakati
Journal:  J Clin Diagn Res       Date:  2016-04-01

3.  Economic burden of beta-thalassemia/Hb E and beta-thalassemia major in Thai children.

Authors:  Arthorn Riewpaiboon; Issarang Nuchprayoon; Kitti Torcharus; Kaemthong Indaratna; Montarat Thavorncharoensap; Bang-On Ubol
Journal:  BMC Res Notes       Date:  2010-01-30

Review 4.  The prevention of thalassemia.

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

Review 5.  Hb E/beta-thalassaemia: a common & clinically diverse disorder.

Authors:  Nancy F Olivieri; Zahra Pakbaz; Elliott Vichinsky
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

6.  The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China.

Authors:  Aihua Yin; Bing Li; Mingyong Luo; Longchang Xu; Li Wu; Liang Zhang; Yuanzhu Ma; Tingting Chen; Shuang Gao; Juqing Liang; Hao Guo; Danqing Qin; Jicheng Wang; Tenglong Yuan; Yixia Wang; Wei-wei Huang; Wen-Fei He; Yanxia Zhang; Chang Liu; Sujian Xia; Qingshan Chen; Qingguo Zhao; Xiaozhuang Zhang
Journal:  PLoS One       Date:  2014-02-27       Impact factor: 3.240

7.  A cost-of-illness analysis of β-Thalassaemia major in children in Sri Lanka - experience from a tertiary level teaching hospital.

Authors:  Hamish Reed-Embleton; Savinda Arambepola; Simon Dixon; Behrouz Nezafat Maldonado; Anuja Premawardhena; Mahinda Arambepola; Jahangir A M Khan; Stephen Allen
Journal:  BMC Pediatr       Date:  2020-05-27       Impact factor: 2.125

8.  Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study.

Authors:  Mohammad Sorowar Hossain; Md Mahbub Hasan; Enayetur Raheem; Muhammad Sougatul Islam; Abdullah Al Mosabbir; Mary Petrou; Paul Telfer; Mahbubul H Siddiqee
Journal:  Orphanet J Rare Dis       Date:  2020-02-21       Impact factor: 4.123

  8 in total

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