Home

  • Order to parcel locker

    Order to parcel locker

  • easy pay

    easy pay
  • Oncofertility
  • Reduced price
Genetic Skin Disorders

Genetic Skin Disorders

9780190276478
Print on demand. This item has an extended shipping time. The typical delivery time is 4-8 weeks.
1,597.05 zł
1,437.34 zł Save 159.71 zł Tax included
Lowest price within 30 days before promotion: 1,437.34 zł
Quantity
Available in 4-6 weeks

  Delivery policy

Choose Paczkomat Inpost, Orlen Paczka, DPD or Poczta Polska. Click for more details

  Security policy

Pay with a quick bank transfer, payment card or cash on delivery. Click for more details

  Return policy

If you are a consumer, you can return the goods within 14 days. Click for more details

Description
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 mostrelevant 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 authors 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
Product Details
OUP USA
85270
9780190276478
9780190276478

Data sheet

Publication date
2017
Issue number
1
Cover
hard cover
Pages count
488
Dimensions (mm)
216 x 279
Weight (g)
1860
  • 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-Lef?vre; 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; 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;
Comments (0)

  • Frequently purchased together

    No products available