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Molecular Basis of Developmental Anomalies of the Human Gastrointestinal Tract
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Main description:

Current knowledge of the etiology of congenital malformations of the human gastrointestinal tract is covered in this book, prefaced by some introductory notes on embryological development. Malformations involving the esophagus, stomach, small and large intestine, anus and rectum, pancreas, and hepato-billiary system are covered. There is a focus on covering those malformations for which a molecular genetic etiology is understood, but other causations, including environmental exposures, twinning, and unknown etiology are also included. For completeness, some disorders are included which are not, strictly, malformations, or which do not, strictly, involve the gastrointestinal tract. Such disorders include Hirschsprung disease, congenital diaphragmatic hernia, omphalocele, and gastroschisis. Suggested approaches to clinical evaluation of individuals with gastrointestinal malformations are included.


Contents:

Introduction
Esophagus
Stomach
Pancreas
Hepato-Biliary Tract
Small Intestine
Colon
Anus and Rectum
Disorders of Laterality
Malformation Sequences Involving Organs of the GI Tract of Non-genetic or Unknown Etiology
Non-genetic Etiologies in Congenital Malformations of the Gastrointestinal Tract
Future of Genetic Testing in GI Malformations
Appendix Table
Bibliography
Author Biography


PRODUCT DETAILS

ISBN-13: 9781615047185
Publisher: Morgan & Claypool Publishers
Publication date: December, 2015
Pages: 125
Weight: 333g
Availability: Available
Subcategories: Gastroenterology

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