The Politics of Sickle Cell and Thalassaemia

The Politics of Sickle Cell and Thalassaemia PDF

Author: Elizabeth N. Anionwu

Publisher:

Published: 2001

Total Pages: 184

ISBN-13:

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Sickle cell disorder (SCD) and thalassaemia are inherited blood disorders which have only recently gained serious attention among health professionals and policy makers. In this text, Anionwu (nursing, Thames Valley U.) and Atkin (U. of Leeds) explore issues regarding these disorders in the UK, and the broader problems faced by minority ethnic communities in acquiring adequate health care and support. Coverage includes a clinical introduction to haemoglobinopathies; screening and diagnosing within the context of the "new genetics," including associated ethical dilemmas and problems; general problems faced by patients and their families, and their daily coping strategies; current shortfalls in providing care; examples of existing good practice; strategies and struggles from the historical development of haemoglobinopathy services in the UK; and opportunities and threats for the future. c. Book News Inc.

The EBMT Handbook

The EBMT Handbook PDF

Author: Nicolaus Kröger

Publisher:

Published: 2020-10-08

Total Pages: 688

ISBN-13: 9781013273674

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This Open Access edition of the European Society for Blood and Marrow Transplantation (EBMT) handbook addresses the latest developments and innovations in hematopoietic stem cell transplantation and cellular therapy. Consisting of 93 chapters, it has been written by 175 leading experts in the field. Discussing all types of stem cell and bone marrow transplantation, including haplo-identical stem cell and cord blood transplantation, it also covers the indications for transplantation, the management of early and late complications as well as the new and rapidly evolving field of cellular therapies. This book provides an unparalleled description of current practices to enhance readers' knowledge and practice skills. This work was published by Saint Philip Street Press pursuant to a Creative Commons license permitting commercial use. All rights not granted by the work's license are retained by the author or authors.

Genetics and Global Public Health

Genetics and Global Public Health PDF

Author: Simon M. Dyson

Publisher: Routledge

Published: 2014-06-11

Total Pages: 221

ISBN-13: 1317977424

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Sickle cell and thalassaemia are among the world’s most common genetic conditions. They are especially common in Africa, Brazil, the Caribbean, the Middle East and Asia. They affect all ethnic groups but they particularly impact on minority ethnic groups in North America, Europe and Australasia. Much research has focused on clinical, laboratory and genetic studies of these conditions. Through a wide-ranging selection of readings based on social scientific research into sickle cell and thalassaemia, this book seeks to redress this imbalance. This is important as, through an examination of the different social, economic and cultural contexts of the lives of people living with sickle cell or thalassaemia, the contributors demonstrate that people are more than the sum of their genes and that their life experiences are rarely derived solely from the clinical severity of their condition but depend on the social context of their lives. Genetics and Global Public Health presents a new concluding chapter which highlights the critical nature of social science research for sickle cell and thalassaemia communities, providing key insights into the social contexts of human behaviour and analysing how societal arrangements could change to assist people living with either condition. It will be of great interest to postgraduate and research students as well as professionals working in the field of public health. This book was originally published as a special issue of the journal Ethnicity and Health.

Ethnicity and Screening for Sickle Cell/thalassaemia

Ethnicity and Screening for Sickle Cell/thalassaemia PDF

Author: Simon Dyson

Publisher: Churchill Livingstone

Published: 2005

Total Pages: 220

ISBN-13:

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Screening policies for sickle cell and thalassaemia have only recently been formalized in the UK. This book asks what types of ethnicity information are relevant for health professionals to ask as part of this screening and why. Through extensive use of interview material, the book draws upon the experiences of sickle cell and thalassaemia counsellors who have been at the forefront of understanding in this area. The book: . Demonstrates how best practice for screening in a multi-ethnic society requires us to better understand the myth of 'races', the meanings of concepts such as ethnicity and racialization, and the relation of racism to issues of citizenship, immigration, asylum and nationality. . Shows how learning from best practice for screening could be a model for developing cultural competency across all types of health care provision. . Clarifies, through the use of the biologically-grounded exemplar of sickle cell and thalassaemia, debates of 'race' and ethnicity for those working in social sciences. . Listens to the voices of experience and validates the hitherto unacknowledged achievements of professional women from minoritized ethnic groups. Extensive direct quotations from experienced sickle cell and thalassemia counsellors Explanations of key concepts, such as 'race', ethnicity and racism Explanation of the political, social and historical factors underlying tensions in asking an ethnicity questions Further resources and website information

Prevention of Thalassaemias and Other Haemoglobin Disorders

Prevention of Thalassaemias and Other Haemoglobin Disorders PDF

Author: Galanello Renzo

Publisher:

Published: 2003

Total Pages: 190

ISBN-13: 9789963623396

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Volume 1 of the Prevention Book presents the principles of a programme for the prevention of the thalassaemia and other haemoglobin disorders, including a description of the various types of disorders requiring prenatal diagnosis, the strategies used for carrier screening, and a number of annexes listing upto date epidemiological and mutation data on thalassaemia. This book was written for use in combination with Volume 2, which describes many of the laboratory protocols in great detail.

Disorders of Hemoglobin

Disorders of Hemoglobin PDF

Author: Martin H. Steinberg

Publisher: Cambridge University Press

Published: 2009-08-17

Total Pages: 883

ISBN-13: 0521875196

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Completely revised new edition of the definitive reference on disorders of hemoglobin.

Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies

Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies PDF

Author: Stephan Lobitz

Publisher: MDPI

Published: 2019-10-07

Total Pages: 160

ISBN-13: 3039216147

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Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the International Journal of Neonatal Screening. Sickle cell disease is one of the most common inherited blood disorders, with a huge impact on health care systems due to high morbidity and high mortality associated with the undiagnosed disease. Newborn screening helps to make the diagnosis early and to prevent fatal complications and diagnostic odysseys. This book gives an overview of diagnostic standards in newborn screening for sickle cell disease and examples of existing newborn screening programs.