Spitz's Genodermatoses: A Full Color Clinical Guide to Genetic Skin Disorders
Spitz, Joel L., Hand, Jennifer Lynn, Turbeville, Jackson Glenn
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商品描述
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
- Read directly on your preferred device(s), such as computer, tablet, or smartphone.
- Easily convert to audiobook, powering your content with natural language text-to-speech.
商品描述(中文翻譯)
使用者友好且高度視覺化的方式,Spitz's Genodermatoses: A Clinical Guide to Genetic Skin Disorders, 3rd Edition 非常適合皮膚科醫生、小兒科醫生和家庭醫生用於考試準備和臨床實踐。Jennifer L. Hand、Joel L. Spitz 和 Jackson Glenn Turbeville 醫生提供了這些複雜且具挑戰性的遺傳疾病的完整且插圖豐富的內容,將每種綜合症以易於閱讀的兩頁展開形式呈現,適合深入研究或快速參考。超過 300 張全彩臨床照片和全身圖解增強了每種綜合症的內容覆蓋。
- 特點包括項目符號文本,總結遺傳模式、產前診斷、發病率、出現年齡、發病機制、主要特徵、鑑別診斷、實驗室發現、管理和預後
- 包含顯著更新的內容——遺傳突變、發病機制、預後、臨床要點和管理——以及全新插圖
- 涵蓋新綜合症和之前討論過的綜合症的新名稱,例如表皮溶解性魚鱗病、淺表性魚鱗病、自體隱性先天性魚鱗病、色素性馬賽克症、伴多發性雀斑的 Noonan 綜合症、PIK3CA 相關過度生長綜合症 (PROS)、多發性嬰兒血管瘤 +\- 皮外疾病、Lynch 綜合症、Muir-Torre 變異型和 Kindler 表皮溶解性水泡病
- 包含框選特點,突顯臨床要點,並為材料增添見解和廣度
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