Atlas of genodermatoses. (2015)

• Record Type: Book
• Further Information: Note: Gianluca Tadini, Michela Brena, Carlo Gelmetti, Lidia Pezzani.
• Authors: Tadini, Gianluca; Brena, Michela; Gelmetti, Carlo; Pezzani, Lidia
• Contents: 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; Unilateral Nevoid and Generalized Essential Telangiectasia; Cutis Marmorata Telangiectatica Congenital; Macrocephaly-Capillary Malformations; Phakomatosis Pigmentovascularis; Hemorragic Telangiectasia; Maffucci Syndrome; Blue Rubber Bleb Angioma Syndrome ; Glomuvenus Malformations; Lymphatic Malformations and Lymphedema Syndromes; Generalized Cyanosis, Phlebectases and Soft Skin syndrome; Syndromic hemangiomas syndrome; ; Metabolic Diseases ; Porphyria Cutanea Tarda and Hepatoerythropoietic Porphyria (HEP); Erythropoietic Protoporphyria; Congenital Erythropoietic Porphyria; Hereditary Coproporphyria and Harderoporphyria; Variegate Porfiria; Acrodermatitis Enteropathica; Fabry Disease; Sea-Blue Histiocytosis; Cerebrotendinous Xanthomatosis; Prolidase Deficiency; Methylmalonic Aciduria; Alkaptonuria; ; Complex Malformative Syndromes with Distinctive Cutaneous Signs ; Rubinstein-Taybi Syndrome; Cornelia De Lange Syndrome; Cohen Syndrome; Branchio-Oculofacial Syndrome; Barber-Say Syndrome; Turner’s Syndrome; Down’s Syndrome; Pallister-Killian Syndrome; Encephalocraniocutaneous Lipomatosis; GAPO Syndrome; Cantu Syndrome; Apert Syndrome; H Syndrome; Poland Syndrome; Kabuki Syndrome; Primary Intestinal Lymphangiectasia; Congenital Insensitivity to Pain; Primary Cutaneous Amyloidosis; Frank-ter Haar-Borrone syndrome; Familial Comedones; ; ; Immunodeficiency Disorders ; Primary Immunodeficiency (PID) Syndromes; Ataxia-Telangiectasia; Chediak-Higashi Syndrome; Cartilage-Hair Hypoplasia; Chronic Granulomatous Disease; Chronic Mucocutaneous Candidiasis; APECED Syndrome; Hyper-IgE Syndromes; Hereditary Angioedema; Omenn Syndrome-Severe Combined Immunodeficiencies; Common Variable Immunodeficiency; Wiskott-Aldrich Syndrome; Immunoglobulin Deficiencies; Cyclic Neutropenia; Leukocyte Adhesion Deficiencies; DiGeorge Syndrome; Fanconi Anemia; ; Autoinflammatory Diseases ; Familial Chilblain Lupus-Aicardi-Goutières complex; Familial Chilblain Lupus; Aicardi-Goutières Syndrome; Monogenic Autoinflammatory Diseases; ; Overgrowth Syndromes ; Proteus Syndrome; CLOVES Syndrome; Beckwith-Wiedemann Syndrome; CLAPO Syndrome ; Klippel-Trénaunay syndrome; Macrocephaly-capillary malformations; ; Genodermatoses Related to Malignancy ; Basal Cell Carcinoma Syndrome; Constitutional Mismatch Repair Deficiency Syndromes; PTEN Hamartoma Syndrome; Gardner Syndrome; Bloom Syndrome; Howel-Evans Syndrome; Multiple Endocrine Neoplasia Syndromes; Peutz-Jeghers Syndrome; Birt-Hogg-Dubé Syndrome; Carney Complex; Bazex-Dupré-Christol Syndrome; Epidermodysplasia Verruciformis; Brooke-Spiegler Syndrome; Progressive Mucinous Hystiocytosis; Degos Disease; Rombo Syndrome; ; Cutaneous Mosaicism; Definition ; Pattern of Clinical Presentation of Mosaicism; The Phenomenon of "Twin-Spots"; Mechanisms of Inheritance of Mosaicism; ; Genodermatoses in Dark Skin ; Federica Dassoni, Gianluca Tadini ; Epidermolysis Bullosa; Darier Disease; Ich
• Edition: Second edition
• Publisher Details: Boca Raton : CRC Press
• Publication Date: 2015
• Extent: 1 online resource, illustrations (colour)
• Subjects: 616.5042; Skin -- Diseases -- Genetic aspects -- Atlases
• Languages: English
• ISBNs: 9781466598362; 9781498715843
• Related ISBNs: 9781466598355
• Notes: Note: Description based on CIP data; item not viewed.
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