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Living with Genetic Disorder: The Impact of Neurofibromatosis 1

Autor Joan Ablon
en Limba Engleză Hardback – 29 aug 1999 – vârsta până la 17 ani
A description of the social, educational, and economic impact of living with a neurological genetic disorder, neurofibromatosis 1. The many unpredictable and potentially stigmatizing possible symptoms of NF1, which range from physical disfigurement to severe learning disorders, may have serious consequences in every aspect of daily life. NF1 was for many years wrongly diagnosed as the Elephant Man's Disease.Ablon examines the psychosocial costs of this misdiagnosis and the ways in which stage, screen, and television parlayed The Elephant Man into the personification of the grimmist extreme of ugliness. This portrayal engendered fear and anxiety for affected persons and their families and also had an impact on the scientific and medical communities. Ablon analyzes the factors that affect individual positive adaptation to NF1 and the demands of American society, and offers suggestions for families, support systems, and health care providers for treatment of affected individuals.
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Specificații

ISBN-13: 9780865692879
ISBN-10: 0865692874
Pagini: 216
Dimensiuni: 156 x 235 x 20 mm
Greutate: 0.43 kg
Ediția:New.
Editura: Bloomsbury Publishing
Colecția Praeger
Locul publicării:New York, United States

Notă biografică

JOAN ABLON is Professor Emerita, Medical Anthropology Program, Department of Anthropology, History, and Social Medicine, School of Medicine, University of California, San Francisco. She is the author of Little People in America (Praeger, 1984) and Living with Difference (Praeger, 1988).

Cuprins

IntroductionPsychosocial Issues in Living with NF1Diagnosis and Response of Families of First Generation Adults to Their ConditionIntergenerational SharingThe School Years--The Staging Ground for StigmaGetting and Keeping a JobThe Search for IntimacyMarriage and ChildbearingGender ResponseLiving with UncertaintyThe Specter of "The Elephant Man"StigmaNF Support GroupsMedical ExperiencesImpactConclusionAppendixesReferencesIndex