Sickle Cell Disease: Pathophysiology, Diagnosis, and Management

(Hardback)

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Sickle cell disease is a complex disease with a genetic mutation producing a wide variety of manifestations. It is of great public health importance nationally and internationally. While the conclusions of this study support the generally accepted view on the disease, the book also provides the most recent information and state-of-the-art knowledge on the subject. It presents the genetic, molecular, cellular, metabolic, rheologic, clinical, diagnostic, therapeutic and psychosocial dimensions of sickle cell disease. Its synthesis of micro to macro, molecular to cellular, individual to social relationships provides a comprehensive study of the disease. The book also offers a synthesis of basic science describing genetic, molecular, metabolic and rheologic aspects of sickle cell disease. Clinical aspects including diagnosis and treatment, and psychosocial aspects, covering the interaction of the patient suffering from sickle cell disease with society, are also treated. Physicians, scientists, allied health workers, sociologists, and social workers, epidemiologists and anthropologists as well as administrators of sickle cell centres should find this volume useful. The major aim of the book is to improve understanding of sickle cell disease and to contribute to a better quality of life for those who have the disease or who are at risk of getting it.

Reviews

. . . The book will fill a need for understanding sickle cell anemia and related conditions, particularly by those who care for these patients as part of their daily routine. The book is recommended to medical students and health care providers.-Hemoglobin
Written in a comprehensive and somewhat sophisticated level; recommended for graduate through professional readers.-Choice
"Written in a comprehensive and somewhat sophisticated level; recommended for graduate through professional readers."-Choice
." . . The book will fill a need for understanding sickle cell anemia and related conditions, particularly by those who care for these patients as part of their daily routine. The book is recommended to medical students and health care providers."-Hemoglobin

Author Bio

VIPUL N. MANKAD, a physician scientist and a pediatric hematologist-oncologist, is Louise Lenoir Lock Distinguished Professor and Vice Chairman of Pediatrics. He is a Senior Scientist at the Comprehensive Sickle Cell Center at the University of South Alabama College of Medicine. R. BLAINE MOORE, a biochemist and red cell scientist is an Associate Director and a Scientist at the Comprehensive Sickle Cell Center at the University of South Alabama College of Medicine. He is also an Associate Professor of Pediatrics and Biochemistry at South Alabama.