Gianluca Tadini, MD, Pediatric Dermatology Unit and Pediatric Clinic 1, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of Milan, Milan, Italy, Michela Brena, MD, Post-Graduate School of Dermatology and Venereology, University of Milan, Milan, Italy, Carlo Gelmetti, MD, Chairman of Pediatric Dermatology Unit, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of Milan, Milan, Italy, Lidia Pezzani, MD, Post-Graduate School of Medical Genetics, University of Milan, Milan, Italy.
EDITION STATEMENT
Edition Statement
Second edition
.PUBLICATION, DISTRIBUTION, ETC
Name of Publisher, Distributor, etc.
Boca Raton London CRC Press
Date of Publication, Distribution, etc.
[2015]
PHYSICAL DESCRIPTION
Specific Material Designation and Extent of Item
1
CONTENTS NOTE
Text of Note
Epidermolysis BullosaEpidermolytic EB Junctional EBDermolytic EBKindler SyndromeAcantholytic DiseasesDarier DiseaseHailey Hailey DiseaseIchthyosesNon-Syndromic IchthyosesSyndromic IchthyosesOther Syndromic IchthyosesPalmoplantar KeratodermasEpidermolytic Palmoplantar Keratoderma Keratoderma Hereditaria MutilansLoricrin Keratoderma Greither DiseaseOlmsted SyndromePapillon-Lefevre SyndromeHuriez SyndromeMal De MeledaPunctate Palmoplantar KeratodermaStriate KeratodermaRichner-Hanhart SyndromePainful CallositiesPachydermoperiostosisAcrokeratoelastoidosisNaxos-Carvajal SyndromesCole DiseasePalmoplantar Keratoderma - Congenital Alopecia Syndrome Other Disorders of KeratinizationPorokeratosesKyrle's DiseasePityriasis Rubra Pilaris Poikilodermas and Aging SyndromesDisorders of DNA RepairAging SyndromesLaminopathiesHair DiseasesMarie-Unna HypotrichosisSimplex of the ScalpAlopecia AreataUlerythema OphryogenesTriangular AlopeciaHypotrichosis with Juvenile Macular Dystrophy Localized HypotrichosisHereditary Hypotrichosis and Recurrent Skin VesiclesWoodehouse-Sakati Syndrome Hypertrichosis CongenitaAmbras SyndromeLocalized HypertrichosisZimmermann-Laband SyndromeMonilethrixPili AnnulatiPili TortiWoolly HairUncombable Hair SyndromeSilvery Hair SyndromeMenkes SyndromeAtrichia with Papular LesionsLoose Anagen SyndromeNail DisordersPachyonychia CongenitaNail-Patella-Elbow SyndromeTwenty-Nail DystrophyMalalignment of the Great ToenailsLeukonychiaPterygium Inversum of NailsIso-Kikuchi SyndromeSebocystomatosisSebocystomatosisOral MucosaWhite Sponge Hyperplasia of the mucosaOral-Facial-Digital Syndrome Type INeurocutaneous SyndromesRASopathies Neurofibromatosis type 1 Noonan Syndrome Cardio-facio-cutaneous Syndrome Costello Syndrome LEOPARD Syndrome Neurofibromatosis type 2TSEpidermal Nevi and Epidermal Nevus Syndromes Introduction Epidermal Nevi and Related SyndromesPhakomatosis Pigmentokeratotica Waxy Keratosis of ChildhoodPENS SyndromePEODDNNevoid Follicular MucinosisCHILD SyndromeEctodermal Dysplasias and Related DisordersEctodermal DysplasiasHypohidrotic ED p63-related EDTricho-Dento-Osseous SyndromeWitkop SyndromeEllis-Van Creveld-Weyers Acrofacial Dysostosis ComplexNectinopathies Connexins-related SyndromesClouston Disease Oculo-Dento-Digital Dysplasia (ODDD) KID syndromeEctodermal Dysplasia-Skin Fragility SyndromePure Hair-Nail Ectodermal DysplasiaTrichorhinophalangeal Syndrome Allgrove SyndromeIncontinentia Pigmenti Goltz SyndromeMIDAS SyndromeNaegeli-Franceschetti SyndromeX-Linked Reticulate Pigmentary Disorder with Systemic Manifestations (XLRPD)Disorders of Connective TissueEhlers-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 GyrataFatty Tissue AnomaliesLaunois-Bensaude SyndromeTotal LipodystrophyPartial Lipodystrophy Lipomas, Familial Multiple Lipomatosis and Nevus LipomatosusAplasia CutisAplasia CutisAdams-Oliver syndromeDisorders of PigmentationOculocutaneous Albinisms (OCAS)Hermansky-Pudlak syndrome Cross SyndromeHypomelanosis of Ito PiebaldismWaardenburg SyndromeMcCune-Albright SyndromeLinear And Figurated Hypo- And Hyper-Pigmented NeviMelanocytic Nevi And Related SyndromesSegmental LentiginosisOta NevusCutis TricolorDyschromatosis Symmetrica Hereditaria Vascular DisordersFast-Flow MalformationsSlow-Flow MalformationsOther 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 syndromeMetabolic DiseasesPorphyria Cutanea Tarda and Hepatoerythropoietic Porphyria (HEP)Erythropoietic ProtoporphyriaCongenital Erythropoietic PorphyriaHereditary Coproporphyria and HarderoporphyriaVariegate PorfiriaAcrodermatitis EnteropathicaFabry DiseaseSea-Blue HistiocytosisCerebrotendinous XanthomatosisProlidase DeficiencyMethylmalonic AciduriaAlkaptonuriaComplex Malformative Syndromes with Distinctive Cutaneous SignsRubinstein-Taybi SyndromeCornelia De Lange SyndromeCohen SyndromeBranchio-Oculofacial SyndromeBarber-Say SyndromeTurner's Syndrome Down's SyndromePallister-Killian SyndromeEncephalocraniocutaneous LipomatosisGAPO SyndromeCantu SyndromeApert SyndromeH SyndromePoland SyndromeKabuki SyndromePrimary Intestinal LymphangiectasiaCongenital Insensitivity to PainPrimary Cutaneous Amyloidosis Frank-ter Haar-Borrone syndrome Familial Comedones Immunodeficiency DisordersPrimary 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 SyndromeImmunoglobulin Deficiencies Cyclic Neutropenia Leukocyte Adhesion Deficiencies DiGeorge Syndrome Fanconi AnemiaAutoinflammatory DiseasesFamilial Chilblain Lupus-Aicardi-Goutieres complex Familial Chilblain LupusAicardi-Goutieres SyndromeMonogenic Autoinflammatory DiseasesOvergrowth SyndromesProteus SyndromeCLOVES SyndromeBeckwith-Wiedemann Syndrome CLAPO Syndrome Klippel-Trenaunay syndrome Macrocephaly-capillary malformations Genodermatoses Related to MalignancyBasal Cell Carcinoma SyndromeConstitutional Mismatch Repair Deficiency Syndromes PTEN Hamartoma Syndrome Gardner Syndrome Bloom Syndrome Howel-Evans Syndrome Multiple Endocrine Neoplasia Syndromes Peutz-Jeghers Syndrome Birt-Hogg-Dube Syndrome Carney Complex Bazex-Dupre-Christol Syndrome Epidermodysplasia Verruciformis Brooke-Spiegler Syndrome Progressive Mucinous Hystiocytosis Degos Disease Rombo SyndromeCutaneous Mosaicism DefinitionPattern of Clinical Presentation of MosaicismThe Phenomenon of "Twin-Spots"Mechanisms of Inheritance of MosaicismGenodermatoses in Dark SkinFederica Dassoni, Gianluca TadiniEpidermolysis BullosaDarier DiseaseIchthyosesPalmoplantar KeratodermasDisorders of DNA RepairNail DisordersNeurocutaneous Syndromes Epidermal nevi and Epidermal nevus syndromesDisorders of Connective TissuesDisorders of PigmentationVascular DisordersMetabolic DiseasesGenodermatoses Related to Malignancies
TOPICAL NAME USED AS SUBJECT
Skin -- Diseases -- Genetic aspects.
LIBRARY OF CONGRESS CLASSIFICATION
Class number
RL81
Book number
.
G536
2015
PERSONAL NAME - PRIMARY RESPONSIBILITY
Gianluca Tadini, MD, Pediatric Dermatology Unit and Pediatric Clinic 1, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of Milan, Milan, Italy, Michela Brena, MD, Post-Graduat