Genetic Skin Disorders

Virginia P. Sybert (Autor)

Buch | Hardcover

488 Seiten

2017 | 3rd Revised edition
Oxford University Press Inc (Verlag)
978-0-19-027647-8 (ISBN)

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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

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-Lefèvre
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
Sjögren-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
François 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

Erscheinungsdatum	12.03.2017
Reihe/Serie	Oxford Monographs on Medical Genetics
Verlagsort	New York
Sprache	englisch
Maße	277 x 224 mm
Gewicht	1860 g
Themenwelt	Medizin / Pharmazie ► Medizinische Fachgebiete ► Biomedizin
	Medizin / Pharmazie ► Medizinische Fachgebiete ► Dermatologie
	Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik
ISBN-10	0-19-027647-9 / 0190276479
ISBN-13	978-0-19-027647-8 / 9780190276478
Zustand	Neuware