Genetics of Obesity Syndromes
Series: Oxford Monographs on Medical Genetics;
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46 278 Ft
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Product details:
- Publisher OUP USA
- Date of Publication 9 July 2009
- Number of Volumes BB
- ISBN 9780195300161
- Binding Hardback
- No. of pages304 pages
- Size 163x234x22 mm
- Weight 646 g
- Language English
- Illustrations halftones, figures, and tables 0
Categories
Long description:
Obesity is one of the most important contributing factors to disease throughout the world and is an area of great current interest among researchers and clinicians. The genetics of common obesity is complex, and an important thread through this labyrinth is the study of genetic syndromes in which obesity is a major component. By examining the genetic mechanisms of obesity in these syndromes, the authors will shed new light on the genetics of common obesity. This is the first book on this important and exciting new area and addreses both the molecular and clinical features of the obesity syndromes, providing hard-core information for researchers and practical guidelines for clinicians caring for obese patients.
The book is divided into three sections: the first covers approaches for assessing and investigating the obese individual; the second describes nondysmorphic, monogenic forms of obesity; and the third documents key, multisystem obesity syndromes with various genetic etiologies. It is as much a reference book as it is a manual and will appeal to clinical geneticists, obesity researchers, endocrinologists, nutritionists, and medical biologists.
This is a great reference for both monogenic and multisystem genetic syndromes associated with obesity. This is the first book that I've seen that covers this increasingly important topic in such detail. It is an important book for anyone interested in obesity and its causes.
Table of Contents:
Section I
Introduction
A Practical Guide to the Clinical Assessment and Investigation of Obesity
Section II: Non-Syndromic Obesity
Leptin and Leptin Receptor Deficiency
Pro-opiomelanocortin Deficiency
Prohormone Convertase
Melanocortin 4 Receptor Deficiency
Section III: Syndromic Obesity
Albrights Hereditary Osteodystrophy, Pseudoparathyroidism and Other GNAS Associated Syndromes
The Clinical and Molecular Genetics of Alström Syndrom
The Clinical, Molecular, and Functional Genetics of Bardet-Biedl Syndrome
The Börjeson-Forssman-Lehmann Syndrome
The Cohen Syndrome
Prader-Willi Syndrome
Syndromes with Obesity