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

• Category:  Books  »  Medicine  »  Diseases
• Format: Hardcover   Learn more about the Hardcover format using Tower WIKI.
• Publisher: Elsevier Science Health Science div
• ISBN: 0721606156
• WAPI (Tower ID): 101577503
• Release Date: August 17, 2005
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• Tower.com Sales Rank: #54813 in Books (See Top 100 Books Bestsellers)
• #1462 in Medicine (See Top 100 Medicine Bestsellers)
• #2 in Diseases (See Top 100 Diseases Bestsellers)

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The completely revised and updated New Edition of this definitive textnow in full color! Long known as the source to consult for guidance on diagnosis, prognosis, plan management, and genetic counseling, this easy-to-use reference focuses on the patterns of human defects caused by inborn errors in morphogenesis as opposed to defects caused by mechanical problems. It provides a wealth of information on normal and abnormal morphogenesis * minor anomalies and their relevance * clinical approaches to specific diagnoses * and normal standards of measurement for the entire spectrum of disorders. Each chapter includes a description of the specific abnormalityincluding occasional associated abnormalitiesnatural history, etiology, and references. On opposing pages are several descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality.

• Provides over 1,450 photographs and illustrations to depict each malformationmany from the personal collections of Drs. Smith and Jonesto aid readers in diagnosis.
• Uses a consistent chapter format to help readers quickly and easily find information on any given disorder
• Offers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation.

• Offers a clearer understanding of abnormalities through the use of more than 1,000 new full-color figures and photographs.
• Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.
• Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome * Deleletion 22q13 syndrome * Meier-Gorlin Syndrome * Short 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.
• Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts.

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