Spitz's Genodermatoses (Hardcover)

Joel L. Spitz

ISBN 10: 1451116519 / ISBN 13: 9781451116519

Published by Lippincott Williams and Wilkins, Philadelphia, 2024

About this Item

Hardcover. Specially designed for dermatologists, pediatricians, and family physicians, this user-friendly guide to genetic skin disorders is an ideal resource for both board preparation and clinical practice. To help make learning a difficult subject more efficient and effective, the text takes a user-friendly, visual approach, featuring more than 300 full-color illustrations and a format designed for maximum retention of content. Features: - 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 Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

Seller Inventory # 9781451116519

Bibliographic Details

• Title: Spitz's Genodermatoses (Hardcover)
• Publisher: Lippincott Williams and Wilkins, Philadelphia
• Publication Date: 2024
• Language: English
• ISBN 10: 1451116519
• ISBN 13: 9781451116519
• Binding: Hardcover
• Edition: 3rd Edition
• Condition: new

About this title

Synopsis

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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