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Book Cover
E-book
Author Spitz, Joel L

Title Genodermatoses : a Clinical Guide to Genetic Skin Disorders
Edition 2nd ed
Published Philadelphia : Wolters Kluwer Health, 2011

Copies

Description 1 online resource (420 pages)
Contents Genodermatoses:A Clinical Guide to Genetic Skin Disorders; Foreword; Preface; Acknowledgments; Contributors; Introduction; Contents; Disorders of Cornification; Ichthyosis Vulgaris; X-linked Ichthyosis; Epidermolytic Hyperkeratosis; Lamellar Ichthyosis; Congenital Ichthyosiform Erythroderma (CIE); Harlequin Fetus; Sjögren-Larsson Syndrome; Refsum Syndrome; Conradi-Hünermann Syndrome; CHILD Syndrome; Netherton Syndrome; Erythrokeratoderma Variabilis; KID Syndrome; Diffuse Palmoplantar Keratoderma (PPK); Howel-Evans Syndrome; Vohwinkel Syndrome; Mal de Meleda; Papillon-Lefèvre Syndrome
Richner-Hanhart SyndromeDarier Disease; Epidermal Nevus Syndrome; Suggested Reading; Chapter 2; Disorders of Pigmentation; Oculocutaneous Albinism Type 1 (OCA1); Oculocutaneous Albinism Type II (OCA2); Hermansky-Pudlak Syndrome; Chédiak-Higashi Syndrome; Griscelli Syndrome; Piebaldism; Waardenburg Syndrome; Hypomelanosis of Ito; Incontinentia Pigmenti; LEOPARD Syndrome; Carney Complex; McCune-Albright Syndrome; Neurofibromatosis I; Neurofibromatosis II; Tuberous Sclerosis; Suggested Reading; Disorders of Vascularization; Sturge-Weber Syndrome; Klippel-Trenaunay Syndrome; Cobb Syndrome
Proteus SyndromeBeckwith-Wiedemann Syndrome; Von Hippel-Lindau Syndrome; Ataxia-Telangiectasia; Hereditary Hemorrhagic TelangiectasiaSyndrome; Cutis Marmorata Telangiectatica Congenita; Maffucci Syndrome; Blue Rubber Bleb Nevus Syndrome; Kasabach-Merritt Syndrome; Diffuse Neonatal Hemangiomatosis; PHACE Syndrome; Suggested Reading; Disorders of Connective Tissue; Ehlers-Danlos Syndrome; Marfan Syndrome; Cutis Laxa; Pseudoxanthoma Elasticum; Osteogenesis Imperfecta; Buschke-Ollendorff Syndrome; Focal Dermal Hypoplasia; Lipoid Proteinosis; Progeria; Werner Syndrome; Aplasia Cutis Congenita
Suggested ReadingDisorders With Malignant Potential; Basal Cell Nevus Syndrome; Xeroderma Pigmentosum; Muir-Torre Syndrome; Dyskeratosis Congenita; Gardner Syndrome; Peutz-Jeghers Syndrome; Cowden Syndrome; Multiple Endocrine Neoplasia Type IIb; Birt-Hogg-Dube Syndrome; Suggested Reading; EpidermolysisBullosa; Epidermolysis Bullosa Simplex; Junctional Epidermolysis Bullosa (JEB); Dystrophic Epidermolysis Bullosa; Suggested Reading; Disorders of PorphyrinMetabolism; Porphyria Cutanea Tarda (PCT); Variegate Porphyria (VP); Acute Intermittent Porphyria (AIP); Hereditary Coproporphyria (HCP)
Erythropoietic Protoporphyria (EPP)Congenital Erythropoietic Porphyria (CEP); Hepatoerythropoietic Porphyria (HEP); Suggested Reading; Disorders WithPhotosensitivity; Bloom Syndrome; Rothmund-Thomson Syndrome; Cockayne Syndrome; Trichothiodystrophy; Hartnup Disease; Suggested Reading; Disorders With Immunodeficiency; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; Hyper-Immunoglobulin E Syndrome; Severe Combined Immunodeficiency; Hereditary Angioedema; Suggested Reading; Disorders of Hair and Nails; Menkes' Syndrome; Björnstad Syndrome; Argininosuccinic Aciduria; Monilethrix
Notes Uncombable Hair Syndrome
Print version record
Subject Skin -- Diseases -- Genetic aspects.
Skin -- Diseases -- Genetic aspects.
Form Electronic book
ISBN 9781451166842
1451166842