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Author: David J. Weatherall
Publisher: John Wiley & Sons
ISBN: 0470695943
Category : Medical
Languages : en
Pages : 864
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Book Description
In the new edition of this successful and authoritative book, the thalassaemias are reviewed in detail with respect to their clinical features, cellular pathology, molecular genetics, prevention and treatment. It is aimed at specialists in haematology in the laboratory or clinical setting, particularly in areas where thalassaemia is common either in the native population or in immigrant communities. The fourth edition has been both updated and re-organized. Three new chapters have been added on the link between alpha-thalassaemia and mental retardation, on avoidance and population control and on global epidemiology. Considerable emphasis is placed on molecular pathology reflecting the huge burst of information to have come out of this field in the last few years.
Author: David J. Weatherall
Publisher: John Wiley & Sons
ISBN: 0470695943
Category : Medical
Languages : en
Pages : 864
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Book Description
In the new edition of this successful and authoritative book, the thalassaemias are reviewed in detail with respect to their clinical features, cellular pathology, molecular genetics, prevention and treatment. It is aimed at specialists in haematology in the laboratory or clinical setting, particularly in areas where thalassaemia is common either in the native population or in immigrant communities. The fourth edition has been both updated and re-organized. Three new chapters have been added on the link between alpha-thalassaemia and mental retardation, on avoidance and population control and on global epidemiology. Considerable emphasis is placed on molecular pathology reflecting the huge burst of information to have come out of this field in the last few years.
Author: Makenzie Greene
Publisher: Nova Science Publishers
ISBN: 9781631179549
Category : Thalassemia
Languages : en
Pages : 0
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Book Description
Thalassemia is one of the most common genetic disorders worldwide and presents major public health and social challenges in areas of high incidence. The frequency of this disorder varies considerably with geographic locations and racial groups. Thalassemia refers to a group of inherited hemolytic anemia disorders that involve defects in the synthesis of hemoglobin α- or β-polypeptide chains. It leads to decreased hemoglobin production and hypochromic microcytic anemia associated with erythrocyte dysplasia and destruction. Homozygous β-thalassemia (also known as thalassemia major, Cooley's anemia, or Mediterranean anemia) is associated with the most severe signs and symptoms. Thalassemia major (TM) is a life-threatening condition that commonly manifests during early infancy, after which progressive pallor, severe anemia, and failure to thrive are common. Children with TM often develop feeding problems, recurrent fever, bleeding tendencies (especially epistaxis), susceptibility to infection, pathologic fractures of long bones and vertebrae, endocrine abnormalities, splenomegaly, lack of sexual maturation, and growth retardation. This book discusses cures and treatments available for thalassemia, as well as the causes and the type of long-term health outcomes it may cause.
Author: David Weatherall
Publisher: Oxford University Press
ISBN: 0199565600
Category : Language Arts & Disciplines
Languages : en
Pages : 258
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Book Description
Here is a complete history of Thalassaemia, the most common type of genetic disorder in the human population, and one of the first whose genetic basis was established. Treatment is also discussed as well at an assessment of how molecular approaches are impacting medicine. - Publisher.--
Author: Jude Kamal
Publisher: Xlibris Corporation
ISBN: 1483613178
Category : Biography & Autobiography
Languages : en
Pages : 145
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Book Description
Book Summary: Jude, a normal girl until the age of three, was diagnosed with Beta Thalassemia Major that taught her to live life with passion and to be grateful for all her blessings. During the same year of Judes diagnosis, her sister Sarah was diagnosed with the same genetic blood disorder, leaving both their parents heartbroken. Although Jude hated Thalassemia at times, blamed herself for all the struggles she faced, she made herself believe that enduring pain will make her stronger. Both sisters have kept Thalassemia a secret from their closest friends in order for them not to be treated differently. They were there for each other no matter what challenge they had facing them. It is a heartfelt and touching journey that unravels the unbroken sisterly bond, inner strength and the constant struggle that never seems to end.
Author: Isam Jaber Al-Zwaini
Publisher: BoD – Books on Demand
ISBN: 1789233666
Category : Medical
Languages : en
Pages : 140
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Book Description
Thalassemia is a very common disease first described by pediatrician Thomas Benton Cooley in 1925 who described it in a patient of Italian origin. At that time, it was designated as Cooley's anemia. George Hoyt Whipple, a Nobel prize winner, and W. L. Bradford, a professor of pediatrics at the University of Rochester, coined the term thalassemia in 1936, which in Greek means anemia of the sea (Thalassa means "sea", and emia means "blood"), due to the fact that it is very common in the area of the Mediterranean Sea. This name is actually misleading because it can occur everywhere in the world. Thalassemia is not a single disease; it is rather a group of hereditary disorders of the production of globulin chain of the hemoglobin. Throughout the world, thalassemia affects approximately 4.4 of every 10,000 live births. It represents a major social and emotional impact on the patient and his family and a major burden on health services where the prevalence is high.
Author: D. J. Weatherall
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 186
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Book Description
Author: Martin H. Steinberg
Publisher: Cambridge University Press
ISBN: 0521875196
Category : Medical
Languages : en
Pages : 883
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Book Description
Completely revised new edition of the definitive reference on disorders of hemoglobin.
Author: Robert Wynn
Publisher: Cambridge University Press
ISBN: 1107439361
Category : Medical
Languages : en
Pages : 299
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Book Description
A succinct summary of the key principles and facts that guide the everyday practice of modern, clinical paediatric hematology. Covering all the information necessary for examinations in the topic, this book is ideal for postgraduates studying paediatric hematology, as well as for junior doctors in training.
Author: Galanello Renzo
Publisher:
ISBN: 9789963623396
Category :
Languages : en
Pages : 190
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Book Description
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.
Author: Stephen Byron Shohet
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 352
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Book Description
