Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation)

 Posted on January 18, 2019  |  

Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) cover

Download Smith’s Recognizable Patterns Of Human Malformation Sixth Edition (Smith’s Recognizable Patterns of Human Malformation) PDF EPUB


Author: Kenneth Jones
Pages: 976
Size: 1.898,95 Kb
Publication Date: August 17,2005
Category: Pathophysiology


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The totally revised and up-to-date New Edition of the definitive text―now completely color!
  • Covers 16 additional typically seen disorders, which includes Deletion 1p36 syndrome * Deleletion 22q13 syndrome * Meier-Gorlin Syndrome * Brief Syndrome * 3-C Syndrome * GAPO Syndrome * Lenz Microphthalmia Syndrome * Muenke Craniosynostosis * Torriello-Carey Syndrome * Mandibulo-Acral Syndrome * Mowat-Wilson Syndrome * Ulnar-Mammary Syndrome * Kaufman-McKusick Syndrome * Smith-Maginess Syndrome * Wiedeman-Rautenstrauch Syndrome * and Shprintzen-Golberg Syndrome. It offers an abundance of information on regular and abnormal morphogenesis * minimal anomalies and their relevance * clinical methods to particular diagnoses * and normal criteria of measurement for the whole spectral range of disorders.
    • On opposing pages are a number of descriptive photographs and series drawings of either a person with the abnormality or particular top features of the abnormality.
    • Provides over 1,450 photos and illustrations to depict each malformation―many from the non-public selections of Drs. Smith and Jones―to aid visitors in analysis.
    • Presents an abundance of new Development Charts, plus full revisions to existing Development Charts.
    • Gives a clearer knowledge of abnormalities by using a lot more than 1,000 new full-color statistics and photos.
    • Includes updates for each disorder, with considerable new details on the molecular basis of malformations in addition to new clinical info for most disorders. Long referred to as the foundation to consult for help with diagnosis, prognosis, plan administration, and genetic guidance, this easy-to-use reference targets the patterns of individual defects due to inborn mistakes in morphogenesis instead of defects due to mechanical complications.
    • Runs on the constant chapter format to greatly help readers efficiently find info on any provided disorder
    • Supplies the most current protection on existing disorders and their molecular basis, in addition to the very latest info on just about any genetic or physiological malformation. Each chapter carries a description of the precise abnormality―including occasional connected abnormalities―natural background, etiology, and references.

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