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Spitz's Genodermatoses
A Full Color Clinical Guide to Genetic Skin Disorders
User-friendly and highly visual in approach, Spitz’s Genodermatoses: A Clinical Guide to Genetic Skin Disorders, 3rd Edition, is ideal for dermatologists, pediatricians, and family physicians for both board preparation and clinical practice. Drs. Jennifer L. Hand, Joel L. Spitz, and Jackson Glenn Turbeville provide complete, well-illustrated coverage of these complex and challenging inherited disorders, presenting each syndrome in an easy-to-read, two-page spread in a format designed for either in-depth study or at-a-glance reference. More than 300 full-color clinical photographs and full-body diagrams enhance coverage of each syndrome.
Features bulleted text that summarizes patterns of inheritance, prenatal diagnosis, incidence, age of presentation, pathogenesis, key features, differential diagnosis, laboratory findings, management, and prognosis
Includes significantly updated content—genetic mutations, pathogenesis, prognosis, clinical pearls, and management—as well as new illustrations throughout
Covers new syndromes and new names for previously discussed syndromes, such as Epidermolytic Ichthyosis, Superficial Ichthyosis, Autosomal Recessive Congenital Ichthyosis, Pigmentary Mosaicism, Noonan Syndrome with Multiple Lentigenes, PIK3CA- Related Overgrowth Spectrum (PROS), Multiple Infantile Hemangiomas +\- Extracutaneous Disease, Lynch Syndrome, Muir-Torre variant, and Kindler Epidermolysis Bullosa
Contains boxed features that highlight clinical pearls and add insight and breadth to the material
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Edition
3
ISBN/ISSN
9781451116519
Product Format
Hardcover Book
Trim Size
8.375 x 10.875
Pages
432
Illustration
427
Edition
3
Publication Date
May 17, 2024
Weight
3.25
Joel L. Spitz MD
Associate in Clinical Dermatology, College of Physicians and Surgeons of Columbia University; Assistant in Dermatology, Columbia Presbyterian Hospital, New York, NY
Jennifer Lynn Hand MD
Jackson Glenn Turbeville
20-30% new material -- update genetic mutations, pathogenesis, prognosis, clinical pearls, management Add 5 new entities Update clinical photos under line drawings (~ 20% new) Boxed features highlight clinical pearls and add insight and breadth to the material Bulleted text summarizing the patterns of inheritance, prenatal diagnosis, incidence, age of presentation, pathogenesis, key features, differential diagnosis, laboratory findings, management, and prognosis Each syndrome is presented in easy-to-read, two-page spreads, allowing you to read material in depth or at-a-glance Full body diagrams and clinical photographs of each syndrome
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