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The global problem of genetic disease

Bibliographic Data

ID13922115
AuthorsD J Weatherall (MRC Weatherall Institute of Molecular Medicine, corresponding author)
Year2005
Volume32
Issue2
Pages117-122
Publication date2005-03-01
Open AccessYes
TypeARTICLE
VenueAnnals of Human Biology (JOURNAL)
Journal identifiersISSN: 0301-4460 • E-ISSN: 1464-5033
PublisherInforma (PUBLISHER • GB)
DOI10.1080/03014460500075480
PMID16096206
OpenAlexW2106728389
LanguageEN
Citations received2
References cited2

Inherited haemoglobin disorders will undoubtedly cause an increasing health burden in many developing countries. Although much is known about their molecular pathology and the mechanisms for their phenotypic diversity, many important questions remain, not least the role of the environment in modifying the clinical course. Methods for screening these conditions are now well established and inexpensive and it is vital that they are applied to define the magnitude of the problem that will be posed by these conditions in the future. Similarly, they form the basis for widespread screening and counselling programmes directed at developing prenatal diagnosis expertise where this is not available. Answers to some relatively simple questions about the role of the environment could also make a major difference to the management of the haemoglobin disorders. There is a major case for the development of regional networks to apply such technology as has been developed for the control and prevention of the important haemoglobin disorders, particularly in Asian countries

Biology · Developing country · Disease · Intensive care medicine · Pathology · Risk analysis (engineering · Hemoglobinopathies and Related Disorders · Iron Metabolism and Disorders · Medicine · Prenatal Screening and Diagnostics

  • Genetics and population health

    Open Access•A H Bittles, Wendy N Erber•Annals of Human Biology•2005

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    Open Access•Li Ping Wong, Elizabeth George et al.•Journal of Community Genetics•2011

Citations per year0.1
Citation span2005 - 2011 (7)
Highly citedNo

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