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 t
Epidermolysis Bullosa: Basic and Clinical Aspects
β Scribed by Robin A. J. Eady (auth.), Andrew N. Lin M.D., D. Martin Carter M.D., Ph.D. (eds.)
- Publisher
- Springer-Verlag New York
- Year
- 1992
- Tongue
- English
- Leaves
- 306
- Edition
- 1
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Synopsis
Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients invariably present to the dermatologist for diagnosis and treatment. However, EB is a systemic disease whose management requires input from clinicians in virtually all fields of medicine, including pediatriΒ cians, surgeons, dentists, gastroenterologists, hematologists, otorhinolarynΒ gologists, dietitians, and physical therapists, to name a few. Because EB is a rare disease, few clinicians are familiar with it, and many recoil at the prosΒ pect of caring for individuals covered with blisters caused by a disease they know little about. For patients, insult is thus added to injury and they feel abandoned, neglected, and frustrated. One way to remedy this deplorable situation is to provide clinicians with a compact source of information deΒ tailing the principles of EB diagnosis and treatment. This text seeks to fulfill this role. From 1986-1991, The Rockefeller University Hospital has been the coΒ ordinating center of the National EB Registry. Supported by The National Institutes of Health, this Registry consists of four university centers* commitΒ ted to collecting clinical data concerning diagnosis, treatment, and epidemioΒ logy on all American EB patients. As of April 1992, nearly 1,799 EB patients have enrolled nationwide. The Registry is now in its second five-year phase of operation.
β¦ Table of Contents
Front Matter....Pages i-xiv
Front Matter....Pages 1-1
Current Perspectives and Differential Diagnosis in Epidermolysis Bullosa....Pages 3-15
Front Matter....Pages 17-17
The Basement Membrane Zone at the Dermal β Epidermal Junction of Human Skin....Pages 19-36
Pathology and Pathogenesis of Epidermolysis Bullosa....Pages 37-62
Collagenase and Connective Tissue Remodeling in Recessive Dystrophic Epidermolysis Bullosa....Pages 63-69
Linkage Studies in Epidermolysis Bullosa....Pages 70-74
Epidermolysis Bullosa Acquisita....Pages 75-86
Front Matter....Pages 87-87
Epidermolysis Bullosa Simplex: A Clinical Overview....Pages 89-117
Junctional Epidermolysis Bullosa: A Clinical Overview....Pages 118-134
Recessive Dystrophic Epidermolysis Bullosa: A Clinical Overview....Pages 135-151
Dominant Dystrophic Epidermolysis Bullosa: A Clinical Overview....Pages 152-165
Front Matter....Pages 167-167
Gastrointestinal Aspects of Epidermolysis Bullosa....Pages 169-184
Ophthalmological Aspects of Epidermolysis Bullosa....Pages 185-190
Hematologic Problems in Epidermolysis Bullosa....Pages 191-197
Dental Aspects of Epidermolysis Bullosa....Pages 198-209
Otorhinolaryngologic Aspects of Epidermolysis Bullosa....Pages 210-216
Rheumatologic Aspects of Epidermolysis Bullosa....Pages 217-219
Front Matter....Pages 221-221
Reconstructive Surgery for Patients with Epidermolysis Bullosa....Pages 223-227
Anesthesia for the Epidermolysis Bullosa Patient....Pages 228-234
Prenatal Diagnosis and Genetic Screening for Epidermolysis Bullosa....Pages 235-251
Physical Rehabilitation of Epidermolysis Bullosa Patients....Pages 252-260
Front Matter....Pages 221-221
Nutritional Management of the Epidermolysis Bullosa Patient....Pages 261-266
Medical and Surgical Treatment of the Skin in Epidermolysis Bullosa....Pages 267-280
Nursing Aspects of Epidermolysis Bullosa: A Comprehensive Approach....Pages 281-294
Back Matter....Pages 295-302
β¦ Subjects
Dermatology
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