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.
Le informazioni nella sezione "Riassunto" possono far riferimento a edizioni diverse di questo titolo.
Forewords
1. General Aspects
1.1. Definition
1.2. Molecular Genetic Background with Classifications
1.3. Types of EB
1.4. Diagnosis
1.4.1. Histopathology
1.4.2. Antigen mapping
1.4.3. Electron Microscopy
1.4.4. Mutation Analysis
1.5. Prenatal and Preimplantation Diagnosis
1.6. Epidemiology
1.7. Economics
1.8. Social Aspects
1.9. Inheritance - Genetic Counseling
2. Therapy
2.1. Interdisciplinary management, teledermatology, telemedicine
2.2. Skin
2.2.1. Avoiding blisters - handling of newborns
2.2.2. Cancer
2.2.3. Webbing/Contractures
2.3. Opthalmology
2.4. Gynecology
2.5. Gastro-Intestinal Tract
2.6. Genito-Urinary Tract
2.7. Dentistry
2.8. Ear/Nose/Throat
2.9. Orthopedics
2.10. Physical Therapy
2.11. Psychology and Psyhiatry
2.12. Respiratory Tract
2.13. Surgery
2.14. Pediatrics - Neonatology
2.15. Internal Medicine
2.16. Pain and Itch
2.17. Nutrition
2.18. Wound Healing - Wound Care
2.19. Gene Therapy
2.20. Complementary Medicine
2.21. EB and Sports
2.21. Therapy of aquired Bullous Autoimmune Diseases
Le informazioni nella sezione "Su questo libro" possono far riferimento a edizioni diverse di questo titolo.
Spese di spedizione:
EUR 17,49
Da: Regno Unito a: U.S.A.
Descrizione libro Hardcover. Condizione: New. Codice articolo 6666-LBR-9783211792704
Descrizione libro Condizione: New. Codice articolo 5646793-n
Descrizione libro Condizione: New. Codice articolo 5646793-n
Descrizione libro Condizione: New. First comprehensive presentation of a multidisciplinary approach to the treatment of Epidermolysis BullosaUpdate on the therapy of this inherited diseasePractical reference for day-to-day care and its many complicationsRichly il. Codice articolo 4487995
Descrizione libro HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000. Codice articolo DB-9783211792704
Descrizione libro Hardcover. Condizione: new. Codice articolo 9783211792704
Descrizione libro HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000. Codice articolo DB-9783211792704
Descrizione libro Condizione: New. PRINT ON DEMAND Book; New; Fast Shipping from the UK. No. book. Codice articolo ria9783211792704_lsuk
Descrizione libro Condizione: New. Codice articolo ABLIING23Mar3113020084364
Descrizione libro Buch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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. 360 pp. Englisch. Codice articolo 9783211792704