03441nam a22005295i 4500001001800000003000900018005001700027007001500044008004100059020003700100024003500137050001200172072001600184072002300200072001500223100015100238245013900389250001800528264006900546300005500615336002600670337002600696338003600722347002400758505037100782520103401153650002402187650002302211650003302234650002202267650002402289650002302313650003602336650002202372700008402394700009002478700008402568710003402652773002602686776003602712776003602748776003602784856004602820912001402866912001402880999001702894978-3-031-60788-2DE-He21320251030113240.0cr nn 008mamaa241023s2024    sz |    s    |||| 0|eng d  a97830316078829978-3-031-60788-27 a10.1007/978-3-031-60788-22doi 4aRL1-803 7aMJK2bicssc 7aMED0170002bisacsh 7aMJK2thema1 aMoftah, Nayera.eauthor.0(orcid)0000-0002-2554-85881https://orcid.org/0000-0002-2554-85884aut4http://id.loc.gov/vocabulary/relators/aut98643210aAtlas of Common and Rare Genodermatosesh[electronic resource] /cby Nayera Moftah, May El Samahy, Nadia Abd El Wadood, Monira Waseef.  a1st ed. 2024. 1aCham :bSpringer Nature Switzerland :bImprint: Springer,c2024.  aXIV, 265 p. 295 illus. in color.bonline resource.  atextbtxt2rdacontent  acomputerbc2rdamedia  aonline resourcebcr2rdacarrier  atext filebPDF2rda0 aPreface -- I. Disorders of keratinization -- II. Disorders of pigmentation -- III. Acantholytic disorders -- IV. Dermal disorders -- V. Disorders of hair and nail -- VI. Syndromes with immunodeficiency -- VII. Hamartoneoplastic syndromes -- VIII. Syndromes with defective excision repair -- IX. Syndromes with vascular disorders -- X. Syndromes with premature aging.  aThe management of cutaneous findings in genodermatoses is challenging to the practicing clinician, especially when all hues of skin and skin types are contemplated, and first-line therapies often inadequate. This carefully crafted Atlas includes all sorts of different ethnic skin types, while featuring a wealth of over 1000 commented images collected in more than a decade, including 200 rare genodermatoses, and providing the reader with key points for correct dermatological diagnosis. The contents start with disorders of keratinization and pigmentation, as well as bullous, acantholytic, dermal, hair and nail diseases. Successively, immunodeficiency syndromes and their skin related symptoms, hamartoneoplastic syndromes and defective excision repair syndromes are presented. The addition of vascular disorders, as well as syndromes with premature aging grant full topic coverage. This Atlas of Common and Rare Genodermatoses will be a valued companion to dermatologists and paediatric specialists in their daily practice. 0aDermatology.972926 0aPediatrics.964087 0aImmunologic diseases.972011 0aDiagnosis.96494214aDermatology.97292624aPediatrics.96408724aImmunological Disorders.97201324aDiagnosis.9649421 aEl Samahy, May.eauthor.4aut4http://id.loc.gov/vocabulary/relators/aut9864331 aAbd El Wadood, Nadia.eauthor.4aut4http://id.loc.gov/vocabulary/relators/aut9864341 aWaseef, Monira.eauthor.4aut4http://id.loc.gov/vocabulary/relators/aut9864352 aSpringerLink (Online service)0 tSpringer Nature eBook08iPrinted edition:z978303160787508iPrinted edition:z978303160789908iPrinted edition:z978303160790540uhttps://doi.org/10.1007/978-3-031-60788-2  aZDB-2-SME  aZDB-2-SXM  c64403d64403