Atlas of Genodermatoses (inbunden)
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Inbunden (Hardback)
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2 New edition
CRC Press Inc
5 Tables, color; 1289 Illustrations, color
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Contains 1 Book and 1 Digital (delivered electroni
Atlas of Genodermatoses (inbunden)

Atlas of Genodermatoses

Inbunden Engelska, 2015-06-25
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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 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, hair, and nails. The entry for each disease includes its epidemiology, laboratory findings, genetics, pathogenesis, cutaneous and extracutaneous findings, differential diagnosis, disease course, complications, and follow-up and therapy, where appropriate. In addition to being a clinical primer, this atlas is also a work of scientific research. The new edition rewrites the classification of some diseases, adds some newly described conditions, and updates established information with the latest molecular genetic studies and references. Specialists in both dermatology and pediatrics should find the atlas an invaluable frontline resource in the clinic.
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"Wonderful descriptions, detailed excellent color photographs, fabulous discussions of causative genetic abnormalities, differential diagnoses, treatments, and associated medical complications... I highly recommend it to all dermatologists." - Doody's Reviews Praise for the Previous Edition: "...[T]his atlas parallels the considerable experience accumulated over several decades in the dermatological clinic of Milan ... a user-friendly comprehensive reference tool that will be useful as a bedside companion." European Journal of Dermatology

Övrig information

Gianluca Tadini, MD, Pediatric Dermatology Unit and Pediatric Clinic 1, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of Milan, Italy Michela Brena, MD, Post-Graduate School of Dermatology and Venereology, University of Milan, Italy Carlo Gelmetti, MD, chairman of the Pediatric Dermatology Unit, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of Milan, Italy Lidia Pezzani, MD, Post-Graduate School of Medical Genetics, University of Milan, Italy


Epidermolysis Bullosa Epidermolytic EB Junctional EB Dermolytic EB Kindler Syndrome Acantholytic Diseases Darier Disease Hailey Hailey Disease Ichthyoses Non-Syndromic Ichthyoses Syndromic Ichthyoses Other Syndromic Ichthyoses Palmoplantar Keratodermas Epidermolytic Palmoplantar Keratoderma Keratoderma Hereditaria Mutilans Loricrin Keratoderma Greither Disease Olmsted Syndrome Papillon-Lefevre Syndrome Huriez Syndrome Mal De Meleda Punctate Palmoplantar Keratoderma Striate Keratoderma Richner-Hanhart Syndrome Painful Callosities Pachydermoperiostosis Acrokeratoelastoidosis Naxos-Carvajal Syndromes Cole DiseasePalmoplantar Keratoderma - Congenital Alopecia Syndrome Other Disorders of Keratinization Porokeratoses Kyrle's Disease Pityriasis Rubra Pilaris Poikilodermas and Aging Syndromes Disorders of DNA Repair Aging Syndromes Laminopathies Hair Diseases Marie-Unna Hypotrichosis Simplex of the Scalp Alopecia Areata Ulerythema Ophryogenes Triangular Alopecia Hypotrichosis with Juvenile Macular Dystrophy Localized Hypotrichosis Hereditary Hypotrichosis and Recurrent Skin Vesicles Woodehouse-Sakati Syndrome Hypertrichosis Congenita Ambras Syndrome Localized Hypertrichosis Zimmermann-Laband Syndrome Monilethrix Pili Annulati Pili Torti Woolly Hair Uncombable Hair Syndrome Silvery Hair Syndrome Menkes Syndrome Atrichia with Papular Lesions Loose Anagen Syndrome Nail Disorders Pachyonychia Congenita Nail-Patella-Elbow Syndrome Twenty-Nail Dystrophy Malalignment of the Great Toenails Leukonychia Pterygium Inversum of Nails Iso-Kikuchi Syndrome Sebocystomatosis Sebocystomatosis Oral Mucosa White Sponge Hyperplasia of the mucosa Oral-Facial-Digital Syndrome Type I Neurocutaneous Syndromes RASopathies Neurofibromatosis type 1 Noonan Syndrome Cardio-facio-cutaneous Syndrome Costello Syndrome LEOPARD Syndrome Neurofibromatosis type 2 TS Epidermal Nevi and Epidermal Nevus Syndromes Introduction Epidermal Nevi and Related Syndromes Phakomatosis Pigmentokeratotica Waxy Keratosis of Childhood PENS Syndrome PEODDN Nevoid Follicular Mucinosis CHILD Syndrome Ectodermal Dysplasias and Related Disorders Ectodermal Dysplasias Hypohidrotic ED p63-related ED Tricho-Dento-Osseous Syndrome Witkop Syndrome Ellis-Van Creveld-Weyers Acrofacial Dysostosis Complex Nectinopathies Connexins-related Syndromes Clouston Disease Oculo-Dento-Digital Dysplasia (ODDD) KID syndrome Ectodermal Dysplasia-Skin Fragility Syndrome Pure Hair-Nail Ectodermal Dysplasia Trichorhinophalangeal Syndrome Allgrove Syndrome Incontinentia Pigmenti Goltz Syndrome MIDAS Syndrome Naegeli-Franceschetti Syndrome X-Linked Reticulate Pigmentary Disorder with Systemic Manifestations (XLRPD) Disorders of Connective Tissue Ehlers-Danlos Syndromes Cutis Laxa Syndromes Pseudoxanthoma Elasticum Urbach-Wiethe Disease Marfan Syndrome Loeys-Dietz Syndrome Arterial Tortuosity Syndrome Stickler Syndrome Connective Tissue Nevi Buschke-Ollendorff Syndrome Elastosis Perforans Serpiginosa Michelin Tire Baby Juvenile Hyaline Fibromatosis Cutaneous Mastocytosis Cutaneous Leiomyomatosis Dermochondrocorneal Dystrophy GNAS-Related Syndromes: Osteoma Cutis, Progressive Osseous Heteroplasia, Albright's Hereditary Osteodistrophy Cutis Verticis Gyrata Fatty Tissue Anomalies Launois-Bensaude Syndrome Total Lipodystrophy Partial Lipodystrophy Lipomas, Familial Multiple Lipomatosis and Nevus Lipomatosus Aplasia Cutis Aplasia Cutis Adams-Oliver syndrome Disorders of Pigmentation Oculocutaneous Albinisms (OCAS) Hermansky-Pudlak syndrome Cross Syndrome Hypomelanosis of Ito Piebaldism Waardenburg Syndrome McCune-Albright Syndrome Linear And Figurated Hypo- And Hyper-Pigmented Nevi Melanocytic Nevi And Related Syndromes Segmental Lentiginosis Ota Nevus Cutis Tricolor Dyschromatosis Symmetrica Hereditaria Vascular Disorders Fast-Flow Malformations Slow-Flow Malformations Other Syndromes with Prominent Vascular Signs Von Hippel-Lindau Syndrome Anemic Nevus Unilate