Description

Book 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,

Spitz39s Genodermatoses

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    £170.00

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    RRP £200.00 – you save £30.00 (15%)

    Order before 4pm tomorrow for delivery by Fri 3 Jul 2026.

    A Hardback by Joel L. Spitz

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      Publisher: LWW
      Publication Date: 5/25/2024
      ISBN13: 9781451116519, 978-1451116519
      ISBN10: 1451116519
      Also in:
      Education

      Description

      Book 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,

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