Name: Genetic Skin Disorders By Virginia P. Sybert (Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington)
SKU: 9780190276478
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Genetic Skin Disorders Summary

Genetic Skin Disorders by Virginia P. Sybert (Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington)

This fully revised and updated edition of GENETIC SKIN DISORDERS reflects the most current understanding of the diagnosis, treatment, genetic basis, and differential diagnoses of inherited skin disorders. Organized with the needs of busy clinicians in mind, it offers detailed clinical guidance on the signs, symptoms, mode of inheritance, recurrence risk, and diagnosis of over 300 skin disorders, all in an accessible, at-a-glance format. Annotated bibliographies highlight the most relevant and up-to-date medical literature. Newly compiled lists of support groups, both national and international, for patients and their families supplement the ample resources for medical professionals. Informed by the author's extensive clinical experience and suffused with a distinctive, witty voice, GENETIC SKIN DISORDERS is an ideal companion in the laboratory, clinic, or consulting room. FEATURES Includes both disease-based chapters and an appendix of skin signs that simplifies differential diagnosis for specialists and general practitioners alike More than 800 color photographs illustrate the full spectrum of hair, skin, and nail abnormalities Updated to reflect current classification of inherited skin disorders and the molecular underpinnings of these conditions

Genetic Skin Disorders Reviews

"In the preface, the author asks, 'why another book on inherited skin diseases? Why a book at all in the era of Web crawlers and e-readers?'. My answer is crystal clear: 'No doubt, this textbook is extremely valuable to have in the clinic's library when seeing patients with suspected genodermatosis!" -Acta Dermato-Venereologica

About Virginia P. Sybert (Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington)

Virginia P. Sybert MD is Clinical Professor in Medical Genetics at the University of Washington and a practicing pediatric dermatologist at Group Health Cooperative in Seattle, Washington. She is an international recognized expert in inherited skin disorders.

Contents Preface Acknowledgments Introduction 1. PRACTICAL INHERITANCE 2. DISORDERS OF THE EPIDERMIS: DIFFERENTIATION AND KINETICS Ichthyoses Bullous Congenital Ichthyosiform Erythroderma Harlequin Ichthyosis Ichthyosis Bullosa of Siemens Ichthyosis Hystrix Ichthyosis Vulgaris Lamellar Exfoliation of the Newborn Lamellar Ichthyosis/Nonbullous Congenital Ichthyosiform Erythroderma Netherton Syndrome Peeling Skin Syndrome Restrictive Dermopathy X-linked Recessive Ichthyosis Erythrokeratodermas Erythrokeratodermia Variabilis et Progressiva Pityriasis Rubra Pilaris Acrokeratoderma Acrokeratoelastoidosis Acrokeratosis Verruciformis (Hopf) Hereditary Palmoplantar Keratodermas Hereditary Palmoplantar Keratoderma with Deafness Hereditary Palmoplantar Keratoderma Epidermolytic Hyperkeratosis Hereditary Palmoplantar Keratoderma Howel-Evans Hereditary Palmoplantar Keratoderma Olmsted Hereditary Palmoplantar Keratoderma Punctate Hereditary Palmoplantar Keratoderma Striata Hereditary Palmoplantar Keratoderma Unna-Thost Hereditary Palmoplantar Keratoderma Vohwinkel Keratolytic Winter Erythema Mal de Meleda Papillon-Lefevre Scleroatrophic and Keratotic Dermatosis of the Limbs Porokeratoses Porokeratosis of Mibelli Other Disorders of the Epidermis Absence of Dermatoglyphics Acanthosis Nigricans Darier-White Disease Hereditary Painful Callosities Keratosis Follicularis Spinulosa Decalvans Knuckle Pads Kyrle/Flegel Disease Ulerythema Ophryogenes Syndromic Disorders CHILD Syndrome Chondrodysplasia Punctata Ichthyosis with Hypogonadism KID Syndrome Neu-Laxova Syndrome Neutral Lipid Storage Disease with Ichthyosis Refsum Disease Richner-Hanhart Syndrome Sjogren-Larsson Syndrome Cohesion Epidermolysis Bullosa Epidermolysis Bullosa Simplex Dowling-Meara Epidermolysis Bullosa Simplex Generalized Epidermolysis Bullosa Simplex Localized Epidermolysis Bullosa Junctional Generalized Epidermolysis Bullosa Junctional Generalized Atrophic Benign Epidermolysis Bullosa Dystrophica Cockayne-Touraine Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Epidermolysis Bullosa Dystrophica Pretibial Transient Bullous Dermolysis of the Newborn Hailey-Hailey Disease 3. DISORDERS OF EPIDERMAL APPENDAGES Hair Alopecias Loose Anagen Hair Male Pattern Baldness Marie Unna Syndrome Hirsutism Gingival Fibromatosis and Hypertrichosis Hypertrichosis Lanuginosa Congenita Leprechaunism Localized Hypertrichosis Hair Shaft Abnormalities, Isolated Monilethrix Pili Annulati Pili Torti Pili Trianguli Et Canaliculi Trichorrhexis Invaginata Trichorrhexis Nodosa Woolly Hair Hair Shaft Abnormalities, Syndromic Menkes Disease Trichodentoosseous Syndrome Trichorhinophalangeal Syndrome Trichothiodystrophy Nails Nail Disorders, Isolated Congenital Malalignment of the Great Toenails Familial Dystrophic Shedding of the Nails Leukonychia Twenty-Nail Dystrophy Nail Disorders, Syndromic Nail-Patella Syndrome Onychotrichodysplasia and Neutropenia Pachyonychia Congenita Sweat Glands Hidradenitis Suppurativa Hyperhidrosis Multiple Syringomas Sebaceous Glands Eruptive Vellus Hair Cysts Familial Dyskeratotic Comedones Oral-Facial-Digital Syndrome Type I Steatocystoma Multiplex Ectodermal Dysplasia Syndromes AEC Syndrome Clouston Syndrome EEC Syndrome Focal Facial Dermal Dysplasia Gapo Syndrome Hypohidrotic Ectodermal Dysplasia Tooth and Nail Syndrome 4. DISORDERS OF PIGMENTATION Hyperpigmentation Carney Complex Dowling-Degos Disease Dyskeratosis Congenita Fanconi Anemia H syndrome Hemochromatosis Incontinentia Pigmenti LEOPARD Syndrome Linear and Whorled Nevoid Hypermelanosis McCune-Albright Syndrome Naegeli Syndrome Neurofibromatosis Nevus Phakomatosis Pigmentovascularis Peutz-Jeghers Syndrome Universal Melanosis Hypopigmentation Albinisms Albinism with Deafness Hermansky-Pudlak Syndrome Oculocutaneous Albinism Tyrosinase Negative Oculocutaneous Albinism Tyrosinase Positive Yellow Mutant Albinism Cross Syndrome Hypomelanosis of Ito Piebaldism Premature Canities Vitiligo Waardenburg Syndrome Types 1, 2, 3, and 4 5. DISORDERS OF THE DERMIS Collagen Ainhum Amniotic Bands Buschke-Ollendorff Syndrome Dermatosparaxis Ehlers-Danlos Syndromes Ehlers-Danlos Types I, II, and III Ehlers-Danlos Type IV Ehlers-Danlos Type VI Ehlers-Danlos Type VIII Reactive Perforating Collagenosis Elastin Costello Syndrome Cutis Laxa Pseudoxanthoma Elasticum Vascular Ataxia Telangiectasia Venous Malformations, Multiple Cutaneous and Mucosal Cutis Marmorata Telangiectatica Congenita Fabry Syndrome Familial Flame Nevi Hereditary Glomus Tumors Hereditary Hemorrhagic Telangiectasia Klippel-Trenaunay-Weber Syndrome Maffucci Syndrome Sturge-Weber Syndrome Mixed Aplasia Cutis Congenita Focal Dermal Hypoplasia Tuberous Sclerosis Complex Other Disorders of the Dermis Albright Hereditary Osteodystrophy Cutis Verticis Gyrata Familial Dysautonomia Francois Syndrome Hyaline Fibromatosis Syndrome Lipoid Proteinosis Multiple Pterygia 6. DISORDERS OF SUBCUTANEOUS TISSUE Cerebrotendinous Xanthomatosis Familial Multiple Lipomatosis Familial Symmetric Lipomatosis Fibrodysplasia Ossificans Progressiva Lipogranulomatosis Partial Lipodystrophy Berardinelli-Seip Syndrome 7. LYMPHEDEMA Cholestasis-Lymphedema Syndrome Distichiasis and Lymphedema Hereditary Lymphedema 8. URTICARIA Familial Cold Urticaria Hereditary Angioedema Melkersson-Rosenthal Syndrome Muckle-Wells Syndrome NOMID/CINCA Urticaria Pigmentosa 9. OTHER DISORDERS Congenital Erosive and Vesicular Dermatosis Erythromelalgia Michelin Tire Baby Stiff Skin 10. TUMORS/HAMARTOMAS Basal Cell Nevus Syndrome Cowden syndrome Cylindromatosis Dysplastic Nevus Syndrome Epidermal Nevus Gardner Syndrome Giant Congenital Nevus Hereditary Keratoacanthomas Hereditary Leiomyomatosis and Renal Cancer Infantile Myofibromatosis Multiple Endocrine Neoplasia Types 1, 2/2A, and 2B/3 Pilomatricoma Proteus Syndrome Sebaceous Nevus Syndrome Tumoral Calcinosis 11. METABOLIC DISEASE Porphyrias Congenital Erythropoietic Porphyria Erythropoietic Protoporphyria Hereditary Coproporphyria Porphyria Cutanea Tarda Variegate Porphyria Mucopolysaccharidoses Hunter Syndrome Other Metabolic Disorders Acrodermatitis Enteropathica Alkaptonuria Biotinidase Deficiency Familial Cutaneous Amyloidosis Prolidase Deficiency 12. PREMATURE AGING Cockayne Syndrome De Barsy Syndrome Hallermann-Streiff Syndrome Hutchinson-Gilford Progeria Werner Syndrome 13. PHOTOSENSITIVITY Bloom Syndrome Hartnup Disorder Kindler Syndrome Polymorphous Light Eruption Rothmund-Thomson Syndrome Xeroderma Pigmentosum 14. IMMUNE DEFICIENCY DISEASES Chediak-Higashi Disease Chronic Granulomatous Disease Epidermodysplasia Verruciformis Familial Mucocutaneous Candidiasis Griscelli Syndrome Types 1,2 and 3 Job Syndrome Mucoepithelial Dysplasia Wiskott-Aldrich Syndrome Appendix A: Glossary Appendix B: Differential Diagnosis by Skin Sign Figure Credits Index

Additional information

Sku

NPB9780190276478

ISBN 13

9780190276478

ISBN 10

0190276479

Title

Genetic Skin Disorders by Virginia P. Sybert (Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington)

Author

Virginia P. Sybert (Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, Staff Dermatologist, Group Health Cooperative Clinical Professor, Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington)

Series

Oxford Monographs on Medical Genetics

Condition

New

Binding type

Hardback

Publisher

Oxford University Press Inc

Year published

2017-03-09

Number of pages

488

Prizes

N/A

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Book picture is for illustrative purposes only, actual binding, cover or edition may vary.

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This is a new book - be the first to read this copy. With untouched pages and a perfect binding, your brand new copy is ready to be opened for the first time

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Genetic Skin Disorders Summary

Genetic Skin Disorders Reviews

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Customer Reviews - Genetic Skin Disorders