Front Cover; Contents; Foreword; Preface; Acknowledgments; Illustration credits; Chapter 1: Epidermolysis bullosa; Chapter 2: Acantholytic diseases; Chapter 3: Ichthyoses; Chapter 4: Palmoplantar keratodermas; Chapter 5: Other disorders of keratinization; Chapter 6: Poikilodermas and aging syndromes; Chapter 7: Hair diseases; Chapter 8: Nail disorders; Chapter 9: Sebocystomatosis; Chapter 10: Oral mucosa; Chapter 11: Neurocutaneous syndromes; CHAPTER 12: Epidermal nevi and epidermal nevus syndromes; Chapter 13: Ectodermal dysplasias and related disorders
Chapter 14: Disorders of connective tissueChapter 15: Fatty tissue anomalies; Chapter 16: Aplasia cutis; Chapter 17: Disorders of pigmentation; Chapter 18: Vascular disorders; Chapter 19: Metabolic diseases; Chapter 20: Complex malformative syndromes with distinctive cutaneous signs; Chapter 21: Immunodeficiency disorders; Chapter 22: Autoinflammatory diseases; Chapter 23: Overgrowth syndromes; Chapter 24: Genodermatoses related to malignancy; Chapter 25: Cutaneous mosaicism; Chapter 26: Genodermatoses in dark skin; Back Cover
Summary
Diagnosing a genetic skin disease can sometimes be a difficult task for a dermatologist. This is especially true for genodermatoses-generally considered rare diseases seldom seem by practicing clinicians. As a result, professionals often have little experience with their diagnosis. The Atlas of Genodermatoses presents a unique collection of such cases gathered patiently over the course of the years by the authors. It provides an unsurpassed overview of the major genodermatoses encountered in practice, even if only on rare occasions. This book discusses almost 200 inherited diseases of the skin