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Smith’s Recognizable Patterns of Human Malformation, 8th Edition, 2024

SKU: 9788131270264

Original price was: ₹7,950.00.Current price is: ₹6,260.00.

In Stock

ISBN Number 9788131270264
Main Author Kenneth Lyons Jones
Copyright Year 2024
Edition Number 8th Edition
Format Book – Paperback
Dimensions 27.9 x 21.6 x 2.5 cm
Illustrations more than 1,500 full-color photographs and illustrations
Imprint Elsevier India
Page Count 1088Pages
Weight 2 kg 520 g
Publication Date 1-Jananuary-2024
Stock Status IN STOCK

Long known as the go-to resource for superbly illustrated, up-to-date coverage in this complex field, Smith’s Recognizable Patterns of Human Malformation, 8th Edition, provides a wealth of information on malformation syndromes of environmental and genetic etiology, recognizable disorders of unknown cause, clinical approaches to specific diagnoses, and normal standards of measurement for the entire spectrum of disorders. This award-winning reference is indispensable for clinicians in pediatrics, neonatology, family medicine, and genetics, as well as nurse practitioners and physician assistants—anyone who needs a complete, authoritative, and easy-to-read guide to help accurately diagnose human disorders, establish prognoses, and provide appropriate management and genetic counseling.

Manifestation Key Features Includes an easy-to-read description of each condition: 

Common and occasional abnormalities, natural history, etiology, and references. Opposing pages contain descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality.

Contains new coverage of Hennekam Syndrome, Parkes Weber Syndrome, KBG Syndrome, Kosaki Overgrowth, Malan Syndrome, and much more. Arranges disorders based on similarity in overall features, so you can easily navigate to the correct section and compare/contrast similar disorders.

Features more than 1,500 full-color photographs and illustrations, many from the personal collections of Drs. Smith and Jones, and others from multiple international collaborators.

Provides summarized information in order to understand basic mechanisms of morphogenesis and birth defects and key concepts in genetics and genetic testing—necessary information for counseling patients and parents.

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