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Life with Epidermolysis Bullosa (EB) [electronic resource] : Etiology, Diagnosis, Multidisciplinary Care and Therapy / edited by Jo-David Fine, Helmut Hintner.

Contributor(s): Publisher: Vienna : Springer Vienna, 2009Description: XXI, 338 p. 120 (partly coloured) Figures online resourceContent type:
  • text
Media type:
  • computer
Carrier type:
  • online resource
ISBN:
  • 9783211792711
Subject(s): Genre/Form: Additional physical formats: Printed edition:: No titleDDC classification:
  • 616.5 23
LOC classification:
  • RL1-803
Online resources:
Contents:
Forewords -- General Aspects: Definition; Molecular Genetic Background with Classifications; Types of EB,- Diagnosis; Prenatal and Preimplantation Diagnosis; Epidemiology; Economics; Social Aspects; Inheritance - Genetic Counseling -- Therapy: Interdisciplinary management, teledermatology, telemedicine; Skin; Opthalmology; Gynecology; Gastro-Intestinal Tract; Genito-Urinary Tract; Dentistry; Ear/Nose/Throat; Orthopedics; Physical Therapy; Psychology and Psyhiatry; Respiratory Tract; Surgery; Pediatrics - Neonatology; Internal Medicine; Pain and Itch; Nutrition; Wound Healing - Wound Care; Gene Therapy; Complementary Medicine; EB and Sports; Therapy of aquired Bullous Autoimmune Diseases.-.
In: Springer eBooksSummary: Epidermolysis bullosa (EB) is a heterogenous group of genodermatoses characterized by the formation of blisters and erosions on skin and mucous membrans from birth on. The cause are mutations in the genes of structural proteins of the junction between epidermis and dermis. This book deals with the treatment of this skin disease itself and its many extracutaneous complications. There is no previous book which has been focused on the therapy and it will be based on evidence-based data derived from the world´s largest cohort of inherited EB-patients, the American EB Registry. An important chapter will discuss gene therapy in hereditary EB which has been recently successfully performed within a localized skin site on a single EB patient as a proof-of-principle test. Given its unique collective contents, the monograph will provide the primary source for clinical informations of this oftentimes severe multiorgan disease.
Item type: eBooks
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Forewords -- General Aspects: Definition; Molecular Genetic Background with Classifications; Types of EB,- Diagnosis; Prenatal and Preimplantation Diagnosis; Epidemiology; Economics; Social Aspects; Inheritance - Genetic Counseling -- Therapy: Interdisciplinary management, teledermatology, telemedicine; Skin; Opthalmology; Gynecology; Gastro-Intestinal Tract; Genito-Urinary Tract; Dentistry; Ear/Nose/Throat; Orthopedics; Physical Therapy; Psychology and Psyhiatry; Respiratory Tract; Surgery; Pediatrics - Neonatology; Internal Medicine; Pain and Itch; Nutrition; Wound Healing - Wound Care; Gene Therapy; Complementary Medicine; EB and Sports; Therapy of aquired Bullous Autoimmune Diseases.-.

Epidermolysis bullosa (EB) is a heterogenous group of genodermatoses characterized by the formation of blisters and erosions on skin and mucous membrans from birth on. The cause are mutations in the genes of structural proteins of the junction between epidermis and dermis. This book deals with the treatment of this skin disease itself and its many extracutaneous complications. There is no previous book which has been focused on the therapy and it will be based on evidence-based data derived from the world´s largest cohort of inherited EB-patients, the American EB Registry. An important chapter will discuss gene therapy in hereditary EB which has been recently successfully performed within a localized skin site on a single EB patient as a proof-of-principle test. Given its unique collective contents, the monograph will provide the primary source for clinical informations of this oftentimes severe multiorgan disease.

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