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 seen by practicing clinicians. As a result, professionals often have little experience with their diagnosis. The Atlas of Genodermatoses presents a unique collection of such ca
Epidermolysis Bullosa. Acantholytic Diseases. Ichthyoses. Palmoplantar Keratodermas. Other Disorders of Keratinization. Poikilodermas and Aging Syndromes. Hair Diseases. Nail Disorders. Sebocystomatosis. Oral Mucosa. Neurocutaneous Syndromes. Epidermal Nevi And Epidermal Nevus Syndromes. Ectodermal Dysplasias And Related Disorders. Disorders Of Connective Tissue. Fatty Tissue Anomalies. Aplasia Cutis. Disorders Of Pigmentation. Vascular Disorders. Metabolic Diseases. Complex Malformative Syndromes With Distinctive Cutaneous Signs. Immunodeficiency Disorders. Autoinflammatory Diseases. Overgrowth Syndromes. Genodermatoses Related to Malignancy. Cutaneous Mosaicism. Genodermatoses in Dark Skin.